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Completed Phase 3 Interventional Results available

Studies of Ocular Complications of AIDS (SOCA)--Ganciclovir-Cidofovir CMV Retinitis Trial (GCCRT)

ClinicalTrials.gov ID: NCT00000143

Public ClinicalTrials.gov record NCT00000143. 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 Jul 21, 2026, 12:06 PM EDT

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

Study identification

NCT ID
NCT00000143
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Johns Hopkins Bloomberg School of Public Health
Other
Enrollment
61 participants

Conditions and interventions

Interventions

  • Ganciclovir implant and oral ganciclovir Device
  • Cidofovir intravenous Drug

Device · Drug

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
Apr 30, 1997
Primary completion
May 31, 2000
Completion
May 31, 2000
Last update posted
Mar 13, 2016

1997 – 2000

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Department of Ophthalmology, University of California, Irvine Irvine California 92697-4375
Shiley Eye Center Center, 0946, University of California, San Diego La Jolla California 92093-0946
LAC/USC Medical Center, 5P21 Rand Schrader Clinic Los Angeles California 90033
Jules Stein Eye Institute, University of California, Los Angeles Los Angeles California 90095-7003
Beckman Vision Center, University of California, San Francisco San Francisco California 94143
Bascom Palmer Eye Institute, University of Miami Miami Florida 33136
University of South Florida, MDC Box 21 Tampa Florida 33612-4799
The Emory Clinic, Emory University Atlanta Georgia 30322
Department of Ophthalmology, Northwestern University Chicago Illinois 60611
Division of Infectious Diseases, Indiana University, Indianapolis Indianapolis Indiana 46202-2879
LSU Eye Center, Louisiana State University Medical Center New Orleans Louisiana 70112
The Wilmer Ophthalmological Institute, The Johns Hopkins University School of Medicine Baltimore Maryland 21287-9217
Harvard/BCH AIDS Clinical Trials Unit, Massachusetts General Hospital Boston Massachusetts 02114
UMDNJ-New Jersey Medical School Newark New Jersey 07103-2499
Department of Ophthalmology, New York University Medical Center New York New York 10016
Department of Ophthalmology, New York Hospital-Cornell Medical Center New York New York 10021
Department of Ophthalmology, Mount Sinai School of Medicine New York New York 10029-6574
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599-7030
Cullen Eye Institute, Baylor College of Medicine 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 NCT00000143, 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 Mar 13, 2016 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00000143 live on ClinicalTrials.gov.

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