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Completed Phase 3 Interventional

An Open Trial of Zidovudine (AZT) Treatment of the AIDS Dementia Complex in Patients With AIDS or Low CD4+ Lymphocyte Counts

ClinicalTrials.gov ID: NCT00000709

Public ClinicalTrials.gov record NCT00000709. 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 7, 2026, 4:32 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 provide accurate and complete neurologic assessment of the course of the AIDS dementia complex in patients treated with zidovudine (AZT). The study will determine how frequently patients improve, how long improvement is sustained, and the magnitude and functional significance of improvement. Individuals with AIDS frequently suffer central nervous system (CNS) problems that are characterized by cognitive, motor, and behavioral deficits, in a disorder known as AIDS dementia complex. Clinical experience suggests that its course is often progressive, going from initial symptoms to moderate or severe dementia within several months. Accumulating evidence now suggests that direct brain infection by the HIV virus is the likely cause of the AIDS dementia complex. Case reports suggest that therapy with AZT, which has been shown to be a strong inhibitor of HIV replication in vitro, may alleviate the AIDS dementia complex. This study will help define the natural history of the AIDS dementia complex in treated patients.

Study identification

NCT ID
NCT00000709
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
50 participants

Conditions and interventions

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
Jan 31, 1990
Last update posted
Oct 28, 2021

Ends 1990

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
UCLA CARE Ctr Los Angeles California 90095
Charity Hosp / Tulane Univ Med School New Orleans Louisiana 70112
Louisiana State Univ Med Ctr / Tulane Med School New Orleans Louisiana 70112
Tulane Univ School of Medicine New Orleans Louisiana 70112
Johns Hopkins Hosp Baltimore Maryland 21287
Bellevue Hosp / New York Univ Med Ctr New York New York 10016
Mem Sloan - Kettering Cancer Ctr New York New York 10021
Univ of Rochester Medical Center Rochester New York 14642
Univ of North Carolina Chapel Hill North Carolina 275997215
Univ Hosp of Cleveland / Case Western Reserve Univ Cleveland Ohio 44106
Julio Arroyo West Columbia South Carolina 29169
Univ of Washington Seattle Washington 98105

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 NCT00000709, 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 Oct 28, 2021 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00000709 live on ClinicalTrials.gov.

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