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ClinicalTrials.gov record
Completed Not applicable Interventional

Double-Blind Comparison of the Efficacy of Continued Zidovudine Versus 2',3'-Dideoxyinosine (ddI) (BMY-40900) for the Treatment of Patients With AIDS or AIDS-Related Complex and Increasing Symptomatology Despite Treatment With Zidovudine

ClinicalTrials.gov ID: NCT00002035

Public ClinicalTrials.gov record NCT00002035. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 28, 2026, 5:35 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To compare the efficacy and safety of orally administered didanosine (ddI) with orally administered zidovudine (AZT) in the treatment of patients who exhibit increasing clinical deterioration despite treatment with AZT.

Study identification

NCT ID
NCT00002035
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
300 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Mar 31, 1992
Last update posted
Aug 4, 2011

Ends 1992

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Univ of Arizona / Health Science Ctr Tucson Arizona 85724 —
Yale Univ Med School New Haven Connecticut 06510 —
G E Morey Jr Fort Lauderdale Florida 33316 —
VP Med Services / HHCS Research Institute Inc Orlando Florida 32806 —
AIDS Research Consortium of Atlanta Atlanta Georgia 30308 —
Edward Hines Veterans Administration Hosp Hines Illinois 60141 —
Univ of Kansas School of Medicine Wichita Kansas 67214 —
Harper Hosp Detroit Michigan 48201 —
Albany Med College / AIDS Treatment Ctr Albany New York 12203 —
Med College of Ohio Toledo Ohio 43699 —
Univ of Pennsylvania / HIV Clinic Philadelphia Pennsylvania 19104 —
Univ of Texas Southwestern Med Ctr of Dallas Dallas Texas 75235 —
Univ TX Galveston Med Branch Galveston Texas 775550882 —
Audie L Murphy Veterans Administration Hosp San Antonio Texas 78284 —
Univ of Utah School of Medicine Salt Lake City Utah 84132 —
Dr Stephen L Green Hampton Virginia 23666 —
Milwaukee County Med Complex Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002035, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 4, 2011 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002035 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →