| Study name and trial number | Sponsors |
Country / Sample size |
Criteria | Phase |
Study arms Intervention Control |
Duration / Primary outcome |
|
| Individually randomized controlled trials | |||||||
| TBTC Study 26:Effectiveness and Tolerability of Weekly Rifapentine/Isoniazid for Three Months Versus Daily Isoniazid for Nine Months for the Treatment of Latent Tuberculosis Infection. NCT00023452 | CDC Dept. of Veteran Affairs |
USA Brazil Canada Spain N˜8000 (Enrolling) |
?2 yrs Not pregnant TST+ at high risk of developing TB HIV+ close contacts of culture + TB patients |
III | RPT/INH once weekly for 3 months | INH for 9 months | ?18yrs: Culture+ TB <18yrs: Culture+ or probable (clinical) TB |
| Tuberculosis Prevention for HIV Infected Adults. NCT00057122 | Johns Hopkins University and NIAID | South Africa N˜1148 (enrolment closed) |
Age?18 yrs HIV‐+ TST ?5mm CXR negative for TB |
III | * RPT/INH for 3 months and observed weekly * RIF/INH for 3 months and observed twice weekly * Continuous INH self supervised |
INH self super‐vised for 6 months |
1‐4 yrs follow up Active TB |
| A Randomized, Placebo‐Controlled Study of Limited Vs. Continuous Isoniazid Tuberculosis Preventive Therapy for HIV‐Infected Persons in Botswana NCT00164281 | CDC Botswana MOH USAID |
Botswana N˜1800 (Enrolling) |
?18yrs HIV+ TST + or not pregnant |
IV | Continuous INH | INH for 6 months | Accrual 1yr, follow‐up 24‐36 months Active PTB or ETB |
| Randomized Controlled Trial of 4 Months Rifampin Versus 9 Months INH for the Treatment of Latent TB. NCT00170209 | McGill University | Canada Number not specified |
Age?15yrs TST + Not pregnant HIV+ or other immune suppressed conditions |
IV | RIF for 4 months | INH for 9 months | April 2004 ‐ July 2007 |
| An efficacy study of two preventive therapy studies in HIV‐infected persons in India. NCT00351702 | Tuberculosis Research Centre, India USAID |
India N=650 (enrolment closed) |
?15yrs HIV + |
III | * ETH/IINH for 6 months | INH for 36 months | Follow up 5 yrs Active TB Mortality |