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 @ 12:12 AM
Ignite Modification Date:
2025-12-25 @ 12:12 AM
NCT ID:
NCT00002258
Eligibility Criteria:
Inclusion Criteria
Patients must have:
* HIV seropositivity by Western blot.
* Advanced ARC or AIDS as defined by CDC.
* Cytopenia defined as total peripheral leukocyte count of \< 3,000 cells/mm3 or platelet count of \< 100,000 cells/mm3 or serum hemoglobin \< 10 g/dl.
* Anticipated life expectancy = or \> 6 months.
* Ambulatory.
* Willing to sign informed consent.
* Willing to forego use of any other investigational therapies except ddI.
Prior Medication:
Allowed \> 2 weeks prior to study entry:
* zidovudine.
* Allowed \> 4 weeks prior to study entry:
* systemic cytotoxic chemotherapy; investigational drugs; medications known to be myelosuppressive as ganciclovir, trimethoprim/sulfamethoxazole or dapsone.
* Allowed \> 6 weeks prior to study entry:
* other hemopoietic growth factor treatment as GM-CSF, EPO.
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
* Active opportunistic infection.
* Symptoms of CNS disease referable to HIV infection.
* Dementia or altered mental status that would prohibit giving and understanding informed consent.
Systemic chemotherapy.
* Investigational therapies other than ddI.
* Medications with known myelosuppressive effects such as ganciclovir, trimethoprim/sulfamethoxazole or dapsone or AZT.
* Other hematopoietic growth factor treatments as GM-CSF, G-CSF, or EPO.
Prophylactic therapy for pneumocystis or oral thrush.
* ddI.
* Corticosteroids or topical corticosteroid creams.
Patients may not have:
* Life expectancy \< 6 months.
* Active drug or alcohol abuse.
* Active opportunistic infections.
* Treatment with any other investigational drugs except ddI within 4 weeks of study entry.
* Dementia or altered mental state that prohibits giving informed consent.
* Symptoms of CNS disease referable to HIV infection.
* Major surgery within 4 weeks of study entry.
* History of major pulmonary or cardiac disease.
* History of any prior malignancy other than Kaposi's sarcoma or noninvasive subcutaneous carcinoma.
* Documented allergic disorder such as asthma, history of anaphylaxis, atopy, serum sickness, or bronchospasm.
Not allowed within 2 weeks prior to study entry:
* zidovudine (AZT).
* Not allowed within 4 weeks prior to study entry:
* systemic cytotoxic chemotherapy; investigational drugs other than ddI; medications known to be myelosuppressive as ganciclovir, trimethoprim/sulfamethoxazole or dapsone.
* Not allowed within 6 weeks prior to study entry:
* other hematopoietic growth factor treatment as GM-CSC, G-CSF, EPO.
Radiation therapy or major surgery within 4 weeks of study entry.
Active drug or alcohol abuse.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00002258
Study Brief:
Protocol Section:
NCT00002258