| NCT00001060 |
A Phase I Trial of HIV-1 C4-V3 Polyvalent Peptide Vaccine in HIV-1 Infected Persons |
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| NCT00001059 |
Comparison of Liposomal Doxorubicin Used Alone or in Combination With Bleomycin Plus Vincristine in the Treatment of Kaposi's Sarcoma in Patients With AIDS |
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| NCT00001058 |
A Comparison of Three Drug Combinations Containing Clarithromycin in the Treatment of Mycobacterium Avium Complex (MAC) Disease in Patients With AIDS |
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| NCT00001057 |
The Effectiveness of Two Anti-HIV Treatments in HIV-Infected Patients |
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| NCT00001056 |
A Phase I Multicenter Clinical Trial to Evaluate the Safety and Immunogenicity of Vaccinia Derived HIV-1 Recombinant Envelope Glycoprotein (gp160) of Human Immunodeficiency Virus: Evaluation of a 200-mcg Dose |
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| NCT00001050 |
Study of Women Who Have AIDS |
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| NCT00001035 |
The Safety and Effectiveness of a Two-Drug Combination in the Treatment of Patients With Hepatitis C Plus Advanced HIV Infections |
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| NCT00001034 |
The Safety and Effectiveness of Ganciclovir in the Prevention of Cytomegalovirus (CMV) of the Eyes and Disease of the Stomach and Intestines in Patients With HIV |
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| NCT00001033 |
The Treatment of Tuberculosis in HIV-Infected Patients |
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| NCT00001032 |
A Study of Dideoxycytidine Plus Zidovudine (AZT) in HIV-Infected Children Who Have Taken AZT |
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| NCT00001020 |
A Phase I Study of the Safety and Immunogenicity of rgp120/HIV-1IIIB Vaccine in Healthy Adult Subjects (NOTE: Study Extended ONLY for Subjects Who Have Previously Received rgp120/HIV-1IIIB or rgp120/HIV-1MN on VEU 006 or VEU 006 Rollover Study) |
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| NCT00001018 |
A Study of Letrazuril in the Treatment of AIDS-Related Diarrhea |
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| NCT00001016 |
A Treatment Protocol for the Use of Trimetrexate With Leucovorin Rescue for AIDS Patients With Pneumocystis Carinii Pneumonia and Serious Intolerance to Approved Therapies |
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| NCT00001006 |
A Study of AS-101 in Patients With AIDS or AIDS Related Complex (ARC) |
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| NCT00001005 |
A Study of Zidovudine Plus Interleukin-2 in HIV-Infected Patients Who Have No Symptoms of Infection But Who Have Tender Lymph Nodes |
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| NCT00001004 |
A Study of Tumor Necrosis Factor and Human Interferon-gamma in Patients With AIDS Related Complex |
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| NCT00001003 |
A Study of Pentamidine in the Prevention of Pneumocystis Carinii Pneumonia |
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| NCT00001002 |
A Study of Foscarnet in the Treatment of HIV Infection in Patients Who Have Taken Zidovudine for a Long Time |
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| NCT00001000 |
A Study of Atvogen in Healthy Volunteers and HIV-Infected Patients Who Have No Symptoms of Infection |
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| NCT00000995 |
A Study of AZT Plus Ganciclovir in Patients With AIDS and Cytomegalovirus (CMV) Infection |
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| NCT00000994 |
A Study of AZT in HIV-Infected Patients With AIDS-Related Kaposi's Sarcoma |
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| NCT00000993 |
A Study of Zidovudine in the Prevention of HIV Infection in Individuals Exposed to the Virus |
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| NCT00000992 |
A Study of Itraconazole in Preventing the Return of Histoplasmosis, a Fungal Infection, in Patients With AIDS |
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| NCT00000969 |
A Prospective, Randomized, Open-Label, Comparative Trial of Dideoxyinosine (ddI) Versus Dideoxycytidine (ddC) in HIV-Infected Patients Who Are Intolerant of or Who Have Failed Zidovudine (AZT) Therapy |
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| NCT00000968 |
A Phase I Multicenter Clinical Trial to Evaluate the Safety and Immunogenicity of Vaccinia-Derived HIV-1 Recombinant Envelope Glycoprotein (gp160) |
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| NCT00000967 |
The Safety of Zidovudine Plus Interferon-Alpha in HIV-Infected Children |
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| NCT00000966 |
A Study of Azithromycin Plus Pyrimethamine in the Treatment of a Brain Infection in Patients With AIDS |
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| NCT00000961 |
The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin (HVIG) Plus Zidovudine in HIV-Infected Infants |
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| NCT00000960 |
The Safety and Effectiveness of Zidovudine in HIV-Infected Pregnant Women and Their Infants |
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| NCT00000959 |
Prophylaxis Against Tuberculosis (TB) in Patients With Human Immunodeficiency Virus (HIV) Infection and Suspected Latent Tuberculous Infection |
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| NCT00000958 |
A Placebo-Controlled, Phase I, Pilot Clinical Trial to Evaluate the Safety and Immunogenicity of ENV 2-3, a Yeast-Derived Recombinant Envelope Protein of Human Immunodeficiency Virus-1, in Combination With MTP-PE/MF59 in Individuals With HIV Infection (Placebo Patients Receive MF59 Emulsion Only) |
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| NCT00000957 |
A Phase I Multicenter Clinical Trial to Evaluate the Safety and Immunogenicity of Vaccinia Derived HIV-1 Recombinant Envelope Glycoprotein (gp160) of Human Immunodeficiency Virus: Evaluation of Accelerated Schedules |
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| NCT00000956 |
A Phase I Multicenter Trial to Evaluate the Safety and Immunogenicity of HIV-1 Recombinant Envelope Glycoprotein gp160 |
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| NCT00000951 |
A Study to Compare the Use of Fluconazole as Continuous Therapy Versus Periodic Therapy in HIV-Positive Patients With Recurrent Thrush |
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| NCT00000950 |
Metabolism of Antituberculosis Drugs in HIV-Infected Persons With Tuberculosis |
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| NCT00000935 |
An Evaluation of IV Gamma Globulin As a Method to Improve Kidney Transplant Survival in Patients With End-Stage Renal Disease Who Are Highly Sensitized to Transplant Antigens |
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| NCT00000933 |
Effects of MAC Preventive Therapy on Disease-Causing Bacteria in HIV-Infected Patients: A Substudy of CPCRA 048 |
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| NCT00000932 |
A Study of the Long-Term Outcomes of HIV-Positive Patients |
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| NCT00000920 |
Fortovase (Saquinavir) Given With Low-Dose Ritonavir, Zidovudine, and Lamivudine to HIV-Positive Pregnant Women During and After Pregnancy and to Their Newborns |
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| NCT00000918 |
A Study to Compare The Ability of Different Anti-HIV Drugs to Decrease Viral Load After Nelfinavir (an Anti-HIV Drug)Treatment Failure |
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| NCT00000912 |
A Study on Amprenavir in Combination With Other Anti-HIV Drugs in HIV-Positive Patients |
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| NCT00000905 |
A Study to Evaluate the Effects of Stopping Maintenance Therapy for Cytomegalovirus (CMV) Retinitis After Effective Anti-HIV Therapy |
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| NCT00000904 |
Safety and Effectiveness of Anti-HIV Vaccines in HIV-Negative Adults |
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| NCT00000903 |
Addition of Efavirenz or Nelfinavir to a Lamivudine/Zidovudine/Indinavir HIV Treatment Regimen |
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| NCT00000902 |
A Study on the Management of Combination Anti-HIV Drug Therapy in HIV-Positive Children With Prior Treatment |
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| NCT00000895 |
A Study to Learn More About MAC Disease and the Use of Anti-HIV Drugs in Patients With Advanced HIV Infection |
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| NCT00000894 |
Comparison of Two Drugs, Cidofovir and Ganciclovir, in Treating Patients With AIDS Who Have CMV Retinitis |
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| NCT00000893 |
Safety, Tolerability, and Anti-HIV Activity of DMP 266 (Efavirenz) in Combination With Nelfinavir in HIV-Positive Children |
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| NCT00000892 |
A Study of Several Anti-HIV Drug Combinations in HIV-Infected Patients Who Have Used Indinavir |
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| NCT00000869 |
A Study of Nevirapine for the Prevention of HIV Transmission From Mothers to Their Babies |
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| NCT00000868 |
A Study to Evaluate the Safety and Effectiveness of HIV-1 LAI gp120 (an HIV Vaccine) Given With or Without HIV-1 MN rgp120 (Another HIV Vaccine) to HIV-Negative Volunteers |
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| NCT00000867 |
A Study to Evaluate the Use of Memantine In Combination With Anti-HIV Drugs to Treat AIDS Dementia Complex (ADC) |
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| NCT00000866 |
A Multicenter, Randomized, Placebo-Controlled, Double-Blind Trial to Evaluate the Safety and Immunogenicity of the Therion Recombinant Vaccinia-HIV-1 IIIB ENV/GAG/POL Vaccine (TCB-3B) and MN RGP 120/HIV-1 In Alum. |
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| NCT00000861 |
The Addition of Indinavir to Anti-HIV Treatment in HIV-Infected Patients |
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| NCT00000860 |
The Effects of Treatment for Mycobacterium Avium Complex (MAC) on the Cells of HIV-Infected Patients |
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| NCT00000859 |
A Randomized Trial of the Efficacy and Safety of a Strategy of Starting With Nelfinavir Versus Ritonavir Added to Background Antiretroviral (AR) Nucleoside Therapy in HIV-Infected Individuals With CD4+ Cell Counts Less Than or Equal to 200/mm3 |
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| NCT00000858 |
Detection of Human Immunodeficiency Virus Type 1 (HIV-1) in Vaginocervical Secretions: Correlation With Clinical Status, Virologic and Immunologic Parameters, and the Presence of Other Infections |
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| NCT00000857 |
A Study to Evaluate the Effects of Interleukin-12 (rhIL-12) in HIV-Positive Patients With CD4 Cell Counts Less Than 50 Cells/mm3 or 300-500 Cells/mm3 |
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| NCT00000856 |
A Phase I/II Pilot Treatment Study Of CSF Penetration And Response To Ganciclovir And Foscarnet In CMV Neurologic Disease. |
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| NCT00000851 |
Comparison of Stavudine Used Alone or in Combination With Didanosine in HIV-Infected Children |
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| NCT00000850 |
The Effectiveness of GM-CSF in HIV-Positive Patients Who Are Also Receiving Anti-HIV Therapy |
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| NCT00000835 |
A Multicenter, Randomized, Placebo-Controlled, Double-Blind Trial to Evaluate the Safety and Immunogenicity of an HIV-1 Pseudovirion Vaccine |
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| NCT00000834 |
A Phase I Study of Methotrexate for HIV Infection |
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| NCT00000833 |
A Phase I Study of Combination Therapy With Didanosine (ddI) and Ribavirin in HIV-Infected Children. |
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| NCT00000832 |
A Randomized, Placebo-Controlled, Double-Blinded Phase I Safety and Immunogenicity Trial of Recombinant Envelope Protein, HIV-1 SF-2 rgp120 (BIOCINE), Combined With MF59 in HIV-1 Uninfected Adult Volunteers |
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| NCT00000827 |
A Phase I/II Study of Hyperimmune IVIG in Slowing Progression of Disease in HIV-Infected Children |
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| NCT00000820 |
A Phase II Study of Low-Dose Interleukin-2 by Subcutaneous Injection in Combination With Antiretroviral Therapy Versus Antiretroviral Therapy Alone in Patients With HIV-1 Infection and at Least 3 Months Stable Antiretroviral Therapy |
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| NCT00000818 |
Evaluation of the Changes in HIV-1 Burden in Peripheral Blood and Lymphoid Tissue Following Zidovudine ( AZT ) Treatment in HIV-1-Infected Patients With CD4+ Cells Between 100 and 500 Cells/mm3. |
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| NCT00000806 |
A Phase I Randomized Dose/Formulation Comparison Study of SC-52151 |
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| NCT00000805 |
A Pharmacokinetic and Tolerance Study of Oral Ganciclovir in HIV-Infected Children With Asymptomatic Cytomegalovirus Infection and Low CD4 Cell Counts or Quiescent Cytomegalovirus Disease |
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Description |
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IPD Sharing Statement |
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| NCT00000804 |
A Randomized Trial of L-735,524, An Inhibitor of the HIV Protease Enzyme, and Interleukin-2 in Persons Infected With HIV (NOTE: Only For Patients Who Previously Completed NIAID 93 CC-113) |
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Description |
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| NCT00000803 |
A Phase II Double-Blind Study of Delavirdine Mesylate ( U-90152 ) in Combination With Zidovudine ( AZT ) and/or Didanosine ( ddI ) Versus AZT and ddI Combination Therapy |
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Description |
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| NCT00000802 |
A Randomized, Comparative Study of Daily Dapsone and Daily Atovaquone for Prophylaxis Against PCP in HIV-Infected Patients Who Are Intolerant of Trimethoprim and/or Sulfonamides |
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Description |
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| NCT00000795 |
A Phase I Safety and Immunogenicity Trial of UBI Multivalent HIV-1 Peptide Immunogen in HIV-1 Seronegative Human Subjects |
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Description |
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| NCT00000794 |
Phase II Randomized Open-Label Trial of Atovaquone Plus Pyrimethamine and Atovaquone Plus Sulfadiazine for the Treatment of Acute Toxoplasmic Encephalitis |
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Description |
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| NCT00000793 |
A Phase II/III Double-Blind Study of Amitriptyline and Mexiletine for Painful Neuropathy in HIV Infection |
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Description |
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| NCT00000792 |
A Pharmacologically Guided Phase I/II Study of Daily Orally Administered Synthetic Hypericin in HIV-Infected Subjects |
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Description |
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| NCT00000769 |
A Phase I/II Study of Recombinant Interleukin-4 in AIDS and Kaposi's Sarcoma |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000768 |
A Randomized Comparative Pharmacokinetic Study of Oral Ganciclovir After Treatment With Intravenous Ganciclovir for Cytomegalovirus Gastrointestinal Disease in AIDS Patients |
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Description |
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| NCT00000767 |
A Multicenter, Randomized, Placebo-Controlled, Double-Blind Trial to Evaluate the Safety and Immunogenicity of a Recombinant Vaccinia-HIV-1 IIIB Env/Gag/Pol Vaccine (TBC-3B) |
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Description |
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| NCT00000766 |
CMV Retinitis Retreatment Trial |
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Description |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000761 |
Phase I/II Study of Recombinant Human Interferon-gamma (rIFN-gamma) in HIV-Infected Children |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000760 |
A Randomized Study of Activity, Safety, and Tolerance of Oral Ro 24-7429 (Tat Antagonist) in Patients With HIV Infection |
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Description |
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| NCT00000759 |
Neurodevelopmental and Neurological Study of Infants and Children With HIV-1 Infection and AIDS in Clinical Trials |
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Description |
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| NCT00000758 |
A Phase III Randomized Trial of Topical Vaginal Fluorouracil (5-Fluorouracil, 5-FU) Maintenance Therapy Versus Observation After Standard Treatment for High-Grade Cervical Dysplasia in HIV-Infected Women |
Identification |
Status |
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Description |
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Arms Interventions |
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| NCT00000757 |
A Phase I Multicenter Trial to Evaluate the Safety and Immunogenicity of HIV-1 Recombinant Envelope Glycoprotein gp160 |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000756 |
Evaluation of the Safety and Tolerance of Immunotherapy With Autologous, Ex-Vivo Expanded, HIV-Specific Cytotoxic T-Cells in HIV-Infected Patients With CD4+ Counts Between 100-400/mm3 |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000751 |
A Phase III Randomized, Double-Blind, Controlled Study of the Use of Anti-HIV Immune Serum Globulin (HIVIG) for the Prevention of Maternal-Fetal HIV Transmission in Pregnant Women and Newborns Receiving Zidovudine (AZT) |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000750 |
A Phase III Study to Evaluate the Safety, Tolerance, and Efficacy of Early Treatment With Zidovudine (AZT) in Asymptomatic Infants With HIV Infection |
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Description |
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IPD Sharing Statement |
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| NCT00000735 |
A Clinical Trial To Evaluate the Toxicity and Antiviral Effects of a Range of Doses of Ampligen in p24 Antigen Positive HIV-Infected Patients With AIDS or ARC |
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Description |
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Arms Interventions |
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| NCT00000734 |
Evaluation of the Interaction Between High Dose Sulfamethoxazole/Trimethoprim and Zidovudine |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000733 |
Phase I Pharmacokinetic and Tolerance Study of Ribavirin in Human Immunodeficiency Virus (HIV) - Infected Patients |
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Status |
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Description |
Conditions |
Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000732 |
Evaluation of the Interaction Between Low Dose Sulfamethoxazole-Trimethoprim and Zidovudine |
Identification |
Status |
Sponsor Collaborators |
Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
Contacts Locations |
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IPD Sharing Statement |
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| NCT00000720 |
A Double-Blind, Placebo-Controlled Trial To Evaluate Intravenous Gamma Globulin in Children With Symptomatic HIV Infection Receiving Zidovudine |
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Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000718 |
A Clinical Trial of Alternating and Intermittent Regimens of 2',3'-Dideoxycytidine and 3'-Azido-3'-Deoxythymidine in the Treatment of Patients With AIDS and Advanced ARC |
Identification |
Status |
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Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000705 |
Safety and Effectiveness of Azidothymidine (AZT) in HIV-Positive Patients With Hemophilia |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000704 |
A Multicenter Dose Ranging Clinical Trial of 2',3'-Dideoxycytidine in the Treatment of Patients With AIDS and Advanced ARC. |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000703 |
Chemotherapy and Azidothymidine, With or Without Radiotherapy, for High Grade Lymphoma in AIDS-Risk Group Members |
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Description |
Conditions |
Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000702 |
A Multicenter Placebo-Controlled Double-Blind Trial to Evaluate Azidothymidine (AZT) Treatment of the AIDS Dementia Complex and Central Nervous System (CNS) Human Immunodeficiency Virus (HIV) Infection |
Identification |
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Description |
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| NCT00000695 |
Open Label Phase I Study To Evaluate the Safety of Combination Therapy With AZT and Interferon-Beta in Patients With AIDS Related Kaposi's Sarcoma |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000694 |
A Phase I Trial of Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor (rHuGM-CSF), Recombinant Alpha Interferon and Azidothymidine (AZT) in AIDS-Associated Kaposi's Sarcoma |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000693 |
Suppression of Cytomegalovirus Retinitis Utilizing High Dose Intravenous Acyclovir and Oral Zidovudine in Patients With AIDS |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000692 |
Phase I Rising Dose Tolerability Study of SC-48334 in Patients With Acquired Immunodeficiency Syndrome (AIDS) and Advanced AIDS Related Complex |
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Oversight |
Description |
Conditions |
Arms Interventions |
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IPD Sharing Statement |
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| NCT00000669 |
A Phase I Safety and Pharmacokinetics Study of 2',3'-Dideoxyinosine (ddI) Administered Twice Daily to Infants and Children With AIDS or Symptomatic HIV Infection |
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Description |
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Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000668 |
A Phase I Pharmacokinetic and Tolerance Study of 28-Day Regimens of Oral Ganciclovir |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000667 |
A Phase I/II Dose Escalation Study of Intradermal gp160 to Evaluate Safety, Delayed Type Hypersensitivity (Skin Test) Responses and Immunogenicity in Asymptomatic HIV Seropositive Patients With More Than 400 CD4+ Cells |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000666 |
A Randomized Prospective Study of Pyrimethamine Therapy for Prevention of Toxoplasmic Encephalitis in HIV-Infected Individuals With Serologic Evidence of Latent Toxoplasma Gondii Infection |
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Description |
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| NCT00000661 |
The Pharmacokinetics of Zidovudine and Oxazepam Alone and in Combination in the HIV-Infected Patient |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000660 |
Phase I Study of Weekly Oral VP-16 for AIDS-Associated Kaposi's Sarcoma |
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Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000659 |
A Phase II Trial of rsCD4 and AZT in Patients With AIDS or Advanced AIDS Related Complex (ARC) |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000658 |
A Phase III Randomized Trial of Low-Dose Versus Standard-Dose mBACOD Chemotherapy With rGM-CSF for Treatment of AIDS-Associated Non-Hodgkin's Lymphoma |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000657 |
Comparison of 2',3'-Dideoxyinosine (Didanosine, ddI) and Zidovudine in Therapy of Patients With the AIDS Dementia Complex |
Identification |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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References |
IPD Sharing Statement |
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| NCT00000656 |
A Phase I/II, Open Label Study to Evaluate the Antiviral Potential of Combination Zidovudine and 2' 3'-Dideoxyinosine (Didanosine) in Patients With Asymptomatic HIV Disease |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000651 |
A Randomized, Double Blind, Comparative Study of Dideoxycytidine (ddC) Alone or ddC/AZT Combination Versus Zidovudine (ZDV) Alone in Patients With HIV Infection Who Have Received Prior ZDV Therapy |
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Description |
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Arms Interventions |
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| NCT00000650 |
An Assessment of the In Vivo Biological Effects of Diethyldithiocarbamate (DTC) in HIV-Infected Patients |
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Description |
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Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000635 |
Treatment of Acyclovir-Resistant Mucocutaneous Herpes Simplex Disease in Patients With AIDS: Open Label Pilot Study of Topical Trifluridine |
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Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000634 |
A Pilot Pharmacokinetic Phase I Evaluation of BI-RG-587 in HIV-Infected Children |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000633 |
A Phase I Multicenter Clinical Trial to Evaluate the Safety and Immunogenicity of Immuno-AG Recombinant HIV gp160 in Asymptomatic HIV Seropositive Individuals |
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Oversight |
Description |
Conditions |
Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000632 |
A Phase I Clinical Trial to Evaluate the Safety and Immunogenicity of 100 mcg of Env 2-3 in MF59 |
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Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000627 |
Pilot Study to Determine the Feasibility of Fluconazole for Induction Treatment and Suppression of Relapse of Histoplasmosis in Patients With the Acquired Immunodeficiency Syndrome |
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Status |
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Oversight |
Description |
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Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000620 |
Action to Control Cardiovascular Risk in Diabetes (ACCORD) |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000606 |
National Emphysema Treatment Trial (NETT) |
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Status |
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Oversight |
Description |
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Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000605 |
Estrogen and Graft Atherosclerosis Research Trial (EAGER) |
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Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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References |
IPD Sharing Statement |
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| NCT00000604 |
Influence of CPB Temperature on CABG Morbidity |
Identification |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000603 |
Cord Blood Stem Cell Transplantation Study (COBLT) |
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Status |
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Oversight |
Description |
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Arms Interventions |
Outcomes |
Eligibility |
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References |
IPD Sharing Statement |
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| NCT00000602 |
Pediatric Hydroxyurea in Sickle Cell Anemia (PED HUG) |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000595 |
Evaluation of Subcutaneous Desferrioxamine as Treatment for Transfusional Hemochromatosis |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000594 |
NHLBI Type II Coronary Intervention Study |
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Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000593 |
Viral Activation Transfusion Study (VATS) |
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Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000592 |
Stroke Prevention in Sickle Cell Anemia (STOP 1) |
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Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000569 |
Lung Health Study II |
Identification |
Status |
Sponsor Collaborators |
Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000568 |
Lung Health Study (LHS) I and III |
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Status |
Sponsor Collaborators |
Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000567 |
High Frequency Ventilation in Premature Infants (HIFI) |
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Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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| NCT00000566 |
Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED) |
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Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000561 |
Mode Selection Trial in Sinus Node Dysfunction (MOST) |
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Status |
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Oversight |
Description |
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Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000560 |
Beta-Blocker Evaluation in Survival Trial (BEST) |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000559 |
Women's Estrogen/Progestin Lipid Lowering Hormone Atherosclerosis Regression Trial (WELL-HART) |
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Status |
Sponsor Collaborators |
Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000558 |
Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy (PEACE) |
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Status |
Sponsor Collaborators |
Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000557 |
Enhancing Recovery in Coronary Heart Disease (ENRICHD) Patients |
Identification |
Status |
Sponsor Collaborators |
Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
Contacts Locations |
References |
IPD Sharing Statement |
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| NCT00000556 |
Atrial Fibrillation Follow-up Investigation of Rhythm Management (AFFIRM) |
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Status |
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| NCT00000551 |
Activity Counseling Trial (ACT) |
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| NCT00000550 |
Rapid Early Action for Coronary Treatment (REACT) |
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| NCT00000535 |
Trial of Nonpharmacologic Interventions in Elderly (TONE) |
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| NCT00000534 |
Calcium for Pre-Eclampsia Prevention (CPEP) |
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| NCT00000533 |
Montreal Heart Attack Readjustment Trial (M-HART) |
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| NCT00000532 |
Women's Healthy Lifestyle Project: Cardiovascular Risk Factors and Menopause |
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| NCT00000520 |
Prevention of Coronary Aneurysms in Kawasaki Syndrome |
Identification |
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| NCT00000518 |
Electrophysiologic Study Versus Electrocardiographic Monitoring (ESVEM) |
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| NCT00000512 |
Familial Atherosclerosis Treatment Study |
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Description |
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| NCT00000505 |
Thrombolysis in Myocardial Infarction (TIMI) |
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| NCT00000504 |
Cardiac Arrhythmia Pilot Study (CAPS) |
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| NCT00000503 |
Randomized Clinical Trial of Non-Surgical Reperfusion of the Coronary Arteries |
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| NCT00000502 |
Evaluation of SC-V Versus Conventional CPR |
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| NCT00000495 |
Prevention of Hypertension: A Randomized Trial |
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Description |
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| NCT00000494 |
Management of Patent Ductus in Premature Infants |
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Description |
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| NCT00000493 |
Multicenter Investigation of Limitation of Infarct Size (MILIS) |
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| NCT00000492 |
Beta-Blocker Heart Attack Trial (BHAT) |
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Description |
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| NCT00000469 |
Asymptomatic Carotid Artery Plaque Study (ACAPS) |
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| NCT00000468 |
Myocardial Infarction Triage and Intervention Project (MITI) |
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| NCT00000467 |
Child and Adolescent Trial for Cardiovascular Health (CATCH) |
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IPD Sharing Statement |
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| NCT00000466 |
Postmenopausal Estrogen/Progestin Interventions (PEPI) |
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Description |
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IPD Sharing Statement |
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| NCT00000461 |
Harvard Atherosclerosis Reversibility Project (HARP) |
Identification |
Status |
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Oversight |
Description |
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IPD Sharing Statement |
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| NCT00000460 |
Training Levels Comparison Trial |
Identification |
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Description |
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| NCT00000459 |
Dietary Intervention Study in Children (DISC) |
Identification |
Status |
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Description |
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IPD Sharing Statement |
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| NCT00000458 |
Sertraline and Cognitive Therapy in Depressed Alcoholics |
Identification |
Status |
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Description |
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| NCT00000457 |
Pharmacologic Relapse Prevention for Alcoholic Smokers |
Identification |
Status |
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Description |
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| NCT00000456 |
Behavioral Therapy Plus Naltrexone for Alcoholism |
Identification |
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Description |
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| NCT00000451 |
Drug Therapy for Alcohol Dependence in Alaska Natives (Naltrexone/Sertraline) |
Identification |
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Description |
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| NCT00000450 |
Naltrexone Maintenance Treatment of Alcoholism |
Identification |
Status |
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Description |
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| NCT00000435 |
dnaJ Peptide for Relieving Rheumatoid Arthritis |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000434 |
Impact of Exercise on Older Persons With Osteoarthritis |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000433 |
Blocking Tumor Necrosis Factor in Ankylosing Spondylitis |
Identification |
Status |
Sponsor Collaborators |
Oversight |
Description |
Conditions |
Arms Interventions |
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Eligibility |
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| NCT00000432 |
Lyme Disease Prevention Program |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000427 |
Effects of Parathyroid Hormone in Men With Osteoporosis |
Identification |
Status |
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Oversight |
Description |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000420 |
Safety of Estrogens in Lupus: Birth Control Pills |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000418 |
Psychosocial Treatment for Acute Low Back Pain |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000406 |
Effects of Strength Training on Knee Osteoarthritis |
Identification |
Status |
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Description |
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Eligibility |
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| NCT00000405 |
Effects of Jumping on Growing Bones |
Identification |
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Description |
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Eligibility |
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| NCT00000404 |
Effects of Comprehensive Care for Knee OA |
Identification |
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Description |
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| NCT00000403 |
Doxycycline and OA Progression |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000402 |
Calcium and Bone Mass in Young Females |
Identification |
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Oversight |
Description |
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IPD Sharing Statement |
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| NCT00000395 |
Antifolate Effectiveness in Arthritis |
Identification |
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Description |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000394 |
Acupuncture for Carpal Tunnel Syndrome |
Identification |
Status |
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Description |
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Eligibility |
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| NCT00000393 |
A Phase I Trial of Peptide T: Efficacy for the Neuropsychiatric Complications of Acquired Immunodeficiency Syndrome (AIDS). |
Identification |
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Description |
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| NCT00000392 |
Phase II Study of the Efficacy of Peptide T in HIV-Positive Individuals With Cognitive Impairment. |
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Description |
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| NCT00000369 |
Maintenance Therapies in Bipolar Disorders |
Identification |
Status |
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Description |
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Eligibility |
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| NCT00000368 |
Treatment of Panic Disorder: Long Term Strategies |
Identification |
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Description |
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| NCT00000367 |
Prevention of Suicide in the Elderly |
Identification |
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Description |
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Eligibility |
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| NCT00000361 |
Autoimmunity in Inner Ear Disease |
Identification |
Status |
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Description |
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Arms Interventions |
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Eligibility |
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| NCT00000359 |
Treatments for Benign Paroxysmal Positional Vertigo (BPPV) |
Identification |
Status |
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Description |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000358 |
Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 7 |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000357 |
Buprenorphine Maintenance for Opiate Dependence - 6 |
Identification |
Status |
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Oversight |
Description |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000356 |
Evaluation of L-alpha-acetylmethadol (LAAM) in Methadone Patients - 5 |
Identification |
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Description |
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Arms Interventions |
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IPD Sharing Statement |
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| NCT00000351 |
Cognitive Correlates of Substance Abuse, Part 2 - 16 |
Identification |
Status |
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Description |
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IPD Sharing Statement |
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| NCT00000350 |
Effects of Stimulant Dependence on Human Striatal Dopamine System - 15 |
Identification |
Status |
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Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000335 |
Activity Monitoring Assessment of Opiate Withdrawal - 4 |
Identification |
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Description |
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| NCT00000334 |
Comparison of Buprenorphine and Methadone - 3 |
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Description |
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Eligibility |
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| NCT00000333 |
Evaluation of Benztropine for Cocaine Craving - 2 |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
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Eligibility |
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IPD Sharing Statement |
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| NCT00000332 |
High Dose Nimodipine Treatment Adjunct - 1 |
Identification |
Status |
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Oversight |
Description |
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Arms Interventions |
Outcomes |
Eligibility |
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IPD Sharing Statement |
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| NCT00000328 |
Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment III) - 3 |
Identification |
Status |
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Oversight |
Description |
Conditions |
Arms Interventions |
Outcomes |
Eligibility |
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References |
IPD Sharing Statement |
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