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.