NCT Number: NCT00000700
A Multi-Center Clinical Trial To Evaluate Azidothymidine (AZT) in the Treatment of Human Immunodeficiency Virus (HIV) Infection in Patients With AIDS Post First Episode PCP
To examine the dose of zidovudine (AZT) that was used in the first placebo-controlled study of AZT in AIDS patients as well as a lower dose of AZT in order to determine if the lower dose results in less harmful side effects while still being effective. Previous studies have shown the effectiveness of AZT in AIDS therapy. AZT has been effective in test tube studies at varying doses. There is a need to see if lower doses result in effective therapy with less harmful side effects.
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Notify MeKey information
Conditions
Age range
12 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Los Angeles County - USC Med Ctr, Los Angeles, California, United States
About this study
Previous studies have shown the effectiveness of AZT in AIDS therapy. AZT has been effective in test tube studies at varying doses. There is a need to see if lower doses result in effective therapy with less harmful side effects.
Patients are assigned at random to one of two treatment programs: (1) 1 dose of AZT given orally (PO) for 6 doses per day; (2) 2 doses of AZT PO for 4 weeks followed by 1 dose PO for the remainder of the trial.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Concurrent Medication:
Allowed:
- All concomitant medication to minimum and record.
- Any approved medications can be used to treat an opportunistic infection.
- Dapsone may be used for Pneumocystis carinii pneumonia (PCP).
- Pyrimethamine - sulfadoxine may be used for toxoplasmosis.
- Ganciclovir for cytomegalovirus may be used for maintenance only.
- Prophylactic therapy for PCP.
Concurrent Treatment:
Allowed:
- Local, limited radiation therapy to isolated Kaposi's sarcoma lesions provided total area is < 5 x 5 cm and a 6-MeV electron beam or 90 kV x-ray = or < 3000 rads total is used.
Patients must have:
- HIV seropositivity as confirmed by any federally licensed ELISA test kit.
- Allowed:
- Malignancy in past which has been in complete remission for 1 year without therapy.
Exclusion criteria
Co-existing Condition:
Patients with active opportunistic infections will be excluded.
Concurrent Medication:
Excluded:
- Aspirin on a regular basis or beyond 72 hours without contacting investigator.
- Cimetidine.
- Flurazepam.
- Indomethacin.
- Ranitidine.
- Probenecid.
Patients with the following are excluded:
- Status post-Pneumocystis carinii pneumonia with symptomatic visceral Kaposi's sarcoma (KS) or progression of KS within the month prior to study entry.
- Other concurrent neoplasms other than basal cell carcinoma of the skin.
- Requiring blood transfusions > once per month. Last transfusion cannot have been given within 7 days of entry.
- Active substance abuse. Unwilling to sign informed consent or to be followed at medical center where enrolled for duration of study and follow-up if necessary.
Prior Medication:
Excluded within 2 weeks of study entry:
- Treatment for acute Pneumocystis carinii pneumonia (PCP).
- Excluded within 30 days of study entry:
- Other antiretroviral agents, immunomodulating agents, or corticosteroids.
Prior Treatment:
Excluded within 30 days of study entry:
- Radiation therapy or cytotoxic chemotherapy for Kaposi's sarcoma.
Required:
- Patients must be at least 2 weeks post- therapy status for acute Pneumocystis carinii pneumonia (PCP).
Treatment and study plan
Sponsors and collaborators
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Nih
Registry information
Important dates
- Study completion
- 1990
- First posted
- Aug 31, 2001
- Registry last updated
- Nov 4, 2021
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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