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Completed Phase 3 Interventional

The Treatment of Tuberculosis in HIV-Infected Patients

ClinicalTrials.gov ID: NCT00001033

Public ClinicalTrials.gov record NCT00001033. 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 5, 2026, 12:45 AM EDT

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

Official title

The Treatment of Pulmonary Mycobacterium Tuberculosis in HIV Infection

Brief summary

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

PER 5/30/95 AMENDMENT: To compare the combined rate of failure during therapy and relapse after therapy between two durations of intermittent therapy (6 versus 9 months) for the treatment of pulmonary tuberculosis (TB) in HIV-infected patients. To compare toxicity, survival, and development of resistance in these two regimens. ORIGINAL: To compare the efficacy and safety of induction and continuation therapies for the treatment of pulmonary TB in HIV-infected patients who are either from areas with known high rates of resistance to one or more anti-TB drugs or from areas where TB is expected to be susceptible to commonly used anti-TB drugs. PER 5/30/95 AMENDMENT: In HIV-negative patients, intermittent anti-TB therapy has been shown to be as effective as daily therapy, but the optimal duration of therapy in HIV-infected patients has not been established. ORIGINAL: In some areas of the country, resistance to one or more of the drugs commonly used to treat TB has emerged. Thus, the need to test regimens containing a new drug exists. Furthermore, the optimal duration of anti-TB therapy for HIV-infected patients with TB needs to be determined.

Study identification

NCT ID
NCT00001033
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
650 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
Jun 30, 1997
Last update posted
Nov 3, 2021

Ends 1997

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
USC CRS Los Angeles California 90033
Howard University Hosp., Div. of Infectious Diseases, ACTU Washington D.C. District of Columbia 20059
Univ. of Miami AIDS CRS Miami Florida 33136
Univ. of Hawaii at Manoa, Leahi Hosp. Honolulu Hawaii 96816
Cook County Hosp. CORE Ctr. Chicago Illinois 60612
Johns Hopkins Adult AIDS CRS Baltimore Maryland 21287
SUNY - Buffalo, Erie County Medical Ctr Buffalo New York 14215
NY Univ. HIV/AIDS CRS New York New York 10016
Cornell University A2201 New York New York 10021
Beth Israel Med. Ctr. (Mt. Sinai) New York New York 10029
Univ. of Cincinnati CRS Cincinnati Ohio 45267
Hosp. of the Univ. of Pennsylvania CRS Philadelphia Pennsylvania 19104

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 NCT00001033, 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 Sep 5, 2026

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The complete protocol, eligibility criteria, and contact information for NCT00001033 live on ClinicalTrials.gov.

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