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Completed Phase 4 Interventional

Gradual Initiation of Sulfamethoxazole/Trimethoprim as Primary Pneumocystis Carinii Pneumonia Prophylaxis

ClinicalTrials.gov ID: NCT00000816

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00000816. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 13, 2026, 10:06 PM EST

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Official title

Gradual Initiation of Trimethoprim/Sulfamethoxazole as Primary Pneumocystis Carinii Pneumonia Prophylaxis

Brief summary

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

To determine whether gradual initiation of sulfamethoxazole/trimethoprim (SMX/TMP) reduces the incidence of treatment-limiting adverse reactions compared to the routine initiation of the drugs for Pneumocystis carinii pneumonia (PCP) prophylaxis in HIV-infected patients. Although a number of clinical trials have demonstrated the superiority of SMX/TMP for PCP prophylaxis, the incidence of adverse reactions to this medication is high. In a pilot study in which patients were initiated with SMX/TMP prophylaxis by gradually increasing the dose over 2 weeks, no significant adverse reactions have occurred.

Study identification

NCT ID
NCT00000816
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
370 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
Sep 1996 (Actual)
Last update posted
Nov 4, 2021

Ends 1996

United States locations

U.S. sites
40
U.S. states
17
U.S. cities
29
Facility City State ZIP Site status
USC CRS Los Angeles California 90033 —
Stanford CRS Palo Alto California 94305 —
Ucsf Aids Crs San Francisco California 94110 —
Santa Clara Valley Med. Ctr. San Jose California — —
San Mateo County AIDS Program San Mateo California — —
Harbor-UCLA Med. Ctr. CRS Torrance California 90502 —
University of Colorado Hospital CRS Aurora Colorado 80262 —
Univ. of Florida Jacksonville NICHD CRS Jacksonville Florida 32209 —
Univ. of Miami AIDS CRS Miami Florida 33136 —
Queens Med. Ctr. Honolulu Hawaii 96816 —
Univ. of Hawaii at Manoa, Leahi Hosp. Honolulu Hawaii 96816 —
Northwestern University CRS Chicago Illinois 60611 —
Cook County Hosp. CORE Ctr. Chicago Illinois 60612 —
Rush Univ. Med. Ctr. ACTG CRS Chicago Illinois 60612 —
Indiana Univ. School of Medicine, Infectious Disease Research Clinic Indianapolis Indiana 46202 —
Methodist Hosp. of Indiana Indianapolis Indiana 46202 —
Tulane/LSU Maternal/Child CRS New Orleans Louisiana 70112 —
Johns Hopkins Adult AIDS CRS Baltimore Maryland 21287 —
Massachusetts General Hospital ACTG CRS Boston Massachusetts 02114 —
Bmc Actg Crs Boston Massachusetts 02118 —
Beth Israel Deaconess - East Campus A0102 CRS Boston Massachusetts 02215 —
Beth Israel Deaconess Med. Ctr., ACTG CRS Boston Massachusetts 02215 —
Hennepin County Med. Ctr., Div. of Infectious Diseases Minneapolis Minnesota 55415 —
University of Minnesota, ACTU Minneapolis Minnesota 55455 —
St. Louis ConnectCare, Infectious Diseases Clinic St Louis Missouri 63112 —
Washington U CRS St Louis Missouri — —
Univ. of Nebraska Med. Ctr., Durham Outpatient Ctr. Omaha Nebraska 68198 —
SUNY - Buffalo, Erie County Medical Ctr. Buffalo New York 14215 —
NY Univ. HIV/AIDS CRS New York New York 10016 —
Beth Israel Med. Ctr. (Mt. Sinai) New York New York 10029 —
Univ. of Rochester ACTG CRS Rochester New York — —
Unc Aids Crs Chapel Hill North Carolina 27599 —
Carolinas HealthCare System, Carolinas Med. Ctr. Charlotte North Carolina 28203 —
Regional Center for Infectious Disease, Wendover Medical Center CRS Greensboro North Carolina 27401 —
Univ. of Cincinnati CRS Cincinnati Ohio 45267 —
MetroHealth CRS Cleveland Ohio 44109 —
Case CRS Cleveland Ohio — —
The Ohio State Univ. AIDS CRS Columbus Ohio 43210 —
Hosp. of the Univ. of Pennsylvania CRS Philadelphia Pennsylvania 19104 —
University of Washington AIDS CRS Seattle Washington 98122 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00000816, 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 4, 2021 · Synced Nov 13, 2026

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