TBTC Study 22: Efficacy of Once-Weekly Rifapentine and Isoniazid in Treatment of Tuberculosis

Sponsor
Centers for Disease Control and Prevention (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT00023335
Collaborator
US Department of Veterans Affairs (U.S. Fed)
1,000
23
71
43.5
0.6

Study Details

Study Description

Brief Summary

Primary Objective: To compare, at the completion of the follow-up phase, the clinical and bacteriologic relapse rates associated with the two study regimens.

Secondary Objectives:

To compare the clinical and bacteriologic failure rates of the two study regimens at the completion of the study phase therapy.

To compare the clinical and bacteriologic response rates for the two study regimens among patients who began study phase therapy with signs and symptoms of tuberculosis or cultures positive for M. tuberculosis.

To compare the toxicity associated with the two study regimens by comparing discontinuation rates due to adverse events and occurrence rates of signs and symptoms associated with adverse events during study phase therapy.

To compare mortality rates of the two study regimens. To compare the rates of completion of therapy within 22 weeks for the two study regimens.

To compare the rate of development of drug-resistant tuberculosis in the two study regimens among study patients classified as treatment failures or relapses.

To compare all of the above performance characteristics for the two study regimens in a small subset of HIV seropositive patients.

To compare attitudes and beliefs about participation in this study between patients who complete study therapy and those who fail to complete study therapy.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
TBTC Study 22: Efficacy and Safety of Once-Weekly Rifapentine and Isoniazid Compared to Efficacy and Safety of Once-Weekly Rifapentine and Isoniazid Compared to Twice-Weekly Rifampin and Isoniazid in the Continuation Phase of Therapy for Pulmonary Tuberculosis
Study Start Date :
Apr 1, 1995
Study Completion Date :
Mar 1, 2001

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    • Culture-positive, drug-susceptible pulmonary tuberculosis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Central Arkansas Veterans Health System Little Rock Arkansas United States 72205
    2 LA County/USC Medical Center Los Angeles California United States 90033
    3 University of California, San Francisco San Francisco California United States 94110
    4 Denver Department of Public Health and Hospitals Denver Colorado United States 80204
    5 Washington, D.C. VAMC Washington District of Columbia United States 20422
    6 Chicago VA Medical Center (Lakeside) Chicago Illinois United States 60611
    7 Hines VA Medical Center Hines Illinois United States 60141
    8 Johns Hopkins University School of Medicine Baltimore Maryland United States 21287-0003
    9 Boston Medical Center Boston Massachusetts United States 02118
    10 New Jersey Medical School Newark New Jersey United States 07107-3001
    11 New York University School of Medicine New York New York United States 10016
    12 Columbia University/Presbyterian Medical Center New York New York United States 10032
    13 Harlem Hospital Center New York New York United States 10037
    14 Carolinas Medical Center Charlotte North Carolina United States 28203
    15 Duke University Medical Center Durham North Carolina United States 34222
    16 Nashville VA Medical Center Nashville Tennessee United States 37212-2637
    17 University of North Texas Health Science Center Fort Worth Texas United States 76107-2699
    18 Thomas Street Clinic Houston Texas United States 77009
    19 Audi L. Murphy VA Hospital San Antonio Texas United States 78284
    20 Seattle King County Health Department Seattle Washington United States 98104
    21 University of British Columbia Vancouver British Columbia Canada Canada V5Z 4R4
    22 University of Manitoba Winnipeg Manitoba Canada CANADA R3A 1R8
    23 Montreal Chest Institute McGill University Montreal Quebec Canada H2X 2P4Pq Canada

    Sponsors and Collaborators

    • Centers for Disease Control and Prevention
    • US Department of Veterans Affairs

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00023335
    Other Study ID Numbers:
    • CDC-NCHSTP-1427
    • TBTC Study 22
    First Posted:
    Sep 10, 2001
    Last Update Posted:
    Sep 5, 2005
    Last Verified:
    Sep 1, 2005
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 5, 2005