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Completed Phase 3 Interventional

A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients

ClinicalTrials.gov ID: NCT00000748

Public ClinicalTrials.gov record NCT00000748. 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 22, 2026, 2:00 AM 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
NCT00000748
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
2,500 participants

Conditions and interventions

Interventions

  • Sulfamethoxazole-Trimethoprim Drug

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
Not listed
Primary completion
Not listed
Completion
Oct 31, 1996
Last update posted
Nov 3, 2021

Ends 1996

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Community Consortium of San Francisco San Francisco California 94110
Stanford Univ School of Medicine Stanford California 94305
Denver CPCRA / Denver Public Hlth Denver Colorado 80204
Wilmington Hosp / Med Ctr of Delaware Wilmington Delaware 19899
Veterans Administration Med Ctr / Regional AIDS Program Washington D.C. District of Columbia 20422
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
AIDS Research Alliance - Chicago Chicago Illinois 60657
Louisiana Comm AIDS Rsch Prog / Tulane Univ Med New Orleans Louisiana 70112
Baltimore Trials Baltimore Maryland 21201
Univ of Maryland at Baltimore Baltimore Maryland 21201
Comprehensive AIDS Alliance of Detroit Detroit Michigan 48201
Henry Ford Hosp Detroit Michigan 48202
Southern New Jersey AIDS Cln Trials / Dept of Med Camden New Jersey 08103
North Jersey Community Research Initiative Newark New Jersey 07103
Partners Research Albuquerque New Mexico 87131
Univ Hosp / HIV - ID Clinic Albuquerque New Mexico 87131
Addiction Research and Treatment Corp Brooklyn New York 11201
Clinical Directors Network of Region II New York New York 10011
Harlem AIDS Treatment Group / Harlem Hosp Ctr New York New York 10037
Bronx Lebanon Hosp Ctr The Bronx New York 10456
Portland Veterans Adm Med Ctr / Rsch & Education Grp Portland Oregon 97210
Philadelphia FIGHT Philadelphia Pennsylvania 19107
Richmond AIDS Consortium Richmond Virginia 23298
Univ of Washington / Pacific Med Ctr Seattle Washington 98144

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 NCT00000748, 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 Nov 3, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00000748 live on ClinicalTrials.gov.

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