Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:12 AM
Ignite Modification Date:
2025-12-25 @ 4:12 AM
NCT ID:
NCT00000820
Eligibility Criteria:
Inclusion Criteria
Concurrent Medication:
Allowed:
* PCP prophylaxis.
* Therapy for an opportunistic infection that develops on study, with the exception of foscarnet for CMV disease or resistant Herpes simplex.
* Systemic corticosteroids ONLY IF given for no longer than 21 days for acute PCP.
* Topical corticosteroids to areas separate from a skin test or IL-2 injection site.
* Acyclovir up to 1000 mg/day as maintenance for recurrent genital Herpes.
* Erythropoietin and filgrastim.
* Antiemetics.
* Antibiotics as clinically indicated.
* Elective standard immunizations at week 8 or later.
Concurrent Treatment:
Allowed:
* Local radiation therapy.
Prior Medication: Required:
* Stable, approved antiretroviral therapy for at least 2 months (was 3 months, amended 3/26/96) prior to study entry.
Patients must have:
* HIV seropositivity.
* CD4 count 300 - 700 cells/mm3.
* Stable antiretroviral therapy for at least 2 months (was 3 months, amended 3/26/96) prior to study entry.
* No history of AIDS-defining illness except for limited cutaneous Kaposi's sarcoma.
* Normal EKG (isolated nonspecific ST and T wave changes permitted).
NOTE:
* This protocol is approved for prisoner participation.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
* Malignancy requiring systemic or local cytotoxic chemotherapy.
* Untreated thyroid disease.
* Asthma requiring intermittent or chronic inhalation or systemic therapy.
* Any medical condition that precludes study entry.
Concurrent Medication:
Excluded:
* Antianginal agents such as nitrates, calcium channel blockers, beta blockers, and antiarrhythmics.
* Systemic or local cytotoxic chemotherapy.
* Interferons.
* Interleukins other than study drug.
* Pentoxifylline ( Trental ).
* Acetylcysteine ( NAC ).
* Sargramostim ( GM-CSF ).
* Dinitrochlorobenzene ( DCNB ).
* Thymosin alpha 1.
* Thymopentin.
* Inosiplex ( Isoprinosine ).
* Polyribonucleoside ( Ampligen ).
* Ditiocarb sodium ( Imuthiol ).
* Therapeutic HIV vaccines.
* Investigational antiretroviral agents such as lamivudine ( 3TC ) and tat and protease inhibitors.
* Foscarnet.
* Aspirin.
* Immune globulin ( IVIG ).
* Thalidomide.
* Systemic corticosteroids (permitted for 21 days or less for PCP treatment only).
Concurrent Treatment:
Excluded:
* Ongoing transfusion.
Patients with the following prior conditions are excluded:
* History of autoimmune disease, including inflammatory bowel disease and psoriasis (although autoimmune thyroid disease that is stable is allowed).
* Clinically significant CNS disease or seizures that have been active within 1 year prior to study entry.
Prior Medication:
Excluded:
* IL-2 within 3 months prior to study entry.
* Any immunomodulatory therapy within 4 weeks prior to study entry.
* Foscarnet within 4 weeks prior to study entry.
* Acute therapy for an opportunistic infection within 14 days prior to study entry.
Active alcohol or substance abuse that would compromise study compliance.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00000820
Study Brief:
Protocol Section:
NCT00000820