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Completed Not applicable Interventional

A Randomized, Double-Blind Study of the Efficacy and Safety of Oral Ganciclovir for the Prevention of CMV Disease in People Infected With the Human Immunodeficiency Virus

ClinicalTrials.gov ID: NCT00002095

Public ClinicalTrials.gov record NCT00002095. 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 2, 2026, 6:36 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 evaluate the efficacy of oral ganciclovir in preventing progression to cytomegalovirus (CMV) disease (e.g., CMV retinitis, gastrointestinal CMV disease) in CMV-infected people with HIV infection and CD4 lymphocyte counts \<= 100 cells/mm3. To evaluate the efficacy of this drug in reducing morbidity associated with coinfection by both CMV and HIV.

Study identification

NCT ID
NCT00002095
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
700 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 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 23, 2005

United States locations

U.S. sites
19
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
East Bay AIDS Ctr Berkeley California 94705
Kraus - Beer Med Group Los Angeles California 90028
UCSD San Diego California 92103
Davies Med Ctr / c/o HIV Institute San Francisco California 94114
Mount Zion Med Ctr San Francisco California 94115
San Francisco Veterans Administration Med Ctr San Francisco California 94121
Harbor - UCLA Med Ctr Torrance California 90502
Georgetown Univ Med Ctr Washington D.C. District of Columbia 20007
Community Research Initiative Coral Gables Florida 33146
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
Rush Presbyterian - Saint Luke's Med Ctr / Rush Med Coll Chicago Illinois 60612
Beth Israel Hosp Boston Massachusetts 02215
Kaplan Cancer Ctr / New York Univ Med Ctr New York New York 10016
St Lukes - Roosevelt Hosp Ctr New York New York 10019
Cornell Univ Med College / New York Hosp New York New York 10021
Buckley Braffman Stern Med Associates Philadelphia Pennsylvania 19107
Univ of Pittsburgh / Graduate School of Public Health Pittsburgh Pennsylvania 15261
Oak Lawn Physicians Group Dallas Texas 75219
Infectious Diseases Association of Houston Houston Texas 77030

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 NCT00002095, 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 23, 2005 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002095 live on ClinicalTrials.gov.

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