The RECENT-TB trial is a hybrid effectiveness- implementation trial. The main trial will recruit 1,806 participants who have completed treatment for pulmonary TB. Half (903 participants) will receive 12 weekly doses of isoniazid + rifapentine (3HP) while the other half will not. All participants will be followed up for 2 years after enrolment.
Embedded studies will evaluate if simple blood tests can predict who is most at risk for developing recurrent TB, collect implementation and costing data to inform porential scale up and evaluate the diagnostic performance of a new test (TB-MBLA) for the diagnosis of recurrent TB.