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Completed Not applicable Interventional

The Safety and Effectiveness of Zidovudine Plus Acyclovir in Patients With Early HIV Infection

ClinicalTrials.gov ID: NCT00002290

Public ClinicalTrials.gov record NCT00002290. 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 Oct 21, 2026, 9:46 AM EDT

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

Official title

A Multi-Center, Double-Blind Trial to Evaluate the Safety and Efficacy of Concurrent Retrovir (Zidovudine) and Zovirax (Acyclovir) Therapy in Patients With Early Symptomatic Human Immunodeficiency Virus (HIV) Infection

Brief summary

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

This double-blind, placebo-controlled study is designed to determine the long-term safety and efficacy of concurrent oral Retrovir / Zovirax (AZT and ACV) therapy and oral AZT therapy alone, in the treatment of early symptomatic HIV infection. Efficacy will be evaluated by monitoring the incidence, severity, and time of development of opportunistic infections and other manifestations of advanced symptomatic HIV infection. The effects of the combination and single AZT therapy on immune function and viral replication will also be evaluated. Study participants will be monitored for evidence of toxicity or intolerance to concurrent AZT / ACV administration and AZT therapy alone.

Study identification

NCT ID
NCT00002290
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Glaxo Wellcome
Industry
Enrollment
Not listed

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Not listed
Last update posted
Jun 24, 2005

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Birmingham Veterans Administration Med Ctr / Univ of Alabama Birmingham Alabama 35233 —
Univ of Arizona / Health Science Ctr Tucson Arizona 85724 —
ViRx Inc San Francisco California 94103 —
Georgetown Univ Med Ctr / Main Hosp 4 Washington D.C. District of Columbia 20007 —
Veterans Administration Med Ctr Bay Pines Florida 33504 —
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612 —
Harper Hosp Detroit Michigan 48201 —
Univ of Pennsylvania / HIV Clinic Philadelphia Pennsylvania 19104 —
Vanderbilt School of Medicine Nashville Tennessee 37232 —
Univ TX Galveston Med Branch Galveston Texas 77550 —
Baylor College of Medicine Houston Texas 77030 —
Univ of Utah School of Medicine Salt Lake City Utah 84132 —
Univ of Virginia Health Sciences Ctr Charlottesville Virginia 22908 —
Richmond AIDS Consortium Richmond Virginia 23219 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002290, 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 Jun 24, 2005 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00002290 live on ClinicalTrials.gov.

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