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. 2013 Feb;10(1):18–25. doi: 10.1513/AnnalsATS.201207-038OC

Table 1.

Key features of the Tuberculosis Trials Consortium clinical trials included in this analysis

Trial Study Population Intervention Evaluated Time of Enrollment Timing of Study Visits at which Symptoms Were Assessed Primary Endpoint Duration of Follow-up
Study 22 (11, 12) Pulmonary TB, susceptible to INH and RIF Once-weekly rifapentine plus INH vs. twice-weekly rifampin plus INH in the continuation phase 2 mo (end of the intensive phase of therapy) Time of TB diagnosis (retrospectively); monthly during Months 2–6 of treatment, then at 3, 6, 9, 12, 18, and 24 mo after completing treatment Culture-positive treatment failure or recurrent TB 24 mo after completing treatment
Study 23 (15) Pulmonary or extrapulmonary TB, susceptible to RIF Twice-weekly rifabutin plus INH in the continuation phase At any time during the first 2 mo of treatment Monthly during months 2–6 of treatment, then at 3, 6, 9, 12, 18, and 24 mo after completing treatment Culture-positive treatment failure or recurrent TB 24 mo after completing treatment
Study 27 (13) Smear-positive pulmonary TB, susceptible to RIF Moxifloxacin vs. ethambutol (both in combination with INH, RIF, and PZA) Within 7 d of starting TB treatment Weeks 0, 2, 4, 6, and 8 and then monthly during the remainder of treatment 2-mo sputum culture status Completion of TB therapy
Study 28 (14) Smear-positive pulmonary TB, susceptible to INH and RIF Moxifloxacin vs. INH (both in combination with RIF, PZA, and EMB) Within 7 d of starting TB treatment Weeks 0, 2, 4, 6, and 8 and then monthly during the remainder of treatment 2-mo sputum culture status Completion of TB therapy

Definition of abbreviations: EMB = ethambutol; HIV = human immunodeficiency virus; INH, isoniazid; PZA = pyrazinamide; RIF = rifampin; TB = tuberculosis.