CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 144,000 enrolled
Drug / intervention
Rifampicindrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03662022
NCT03662022Phase 3Completed

Post ExpOsure Prophylaxis for LEprosy in the Comoros and Madagascar

Institute of Tropical Medicine, Belgium·interventional·Posted Sep 7, 2018·Updated Mar 4, 2025

In Brief

A Phase 3 clinical trial evaluating Rifampicin for Leprosy. Completed, enrolled 144,000 participants across 3 sites in 2 countries.

Detailed Summary

This is a cluster randomized trial on effectiveness of different modalities of Single Double Dose of Rifampicin Post-Exposure Prophylaxis (SDDR-PEP) for leprosy in the Comoros (Anjouan and Mohéli) and Madagascar. The study aims to identify which approach to the selection of contacts for post exposure prophylaxis is most effective to reduce incident leprosy, and to Interrupt ongoing transmission from asymptomatic persons in the process of developing multibacillary leprosy.

Study Details

Timeline

Phase 3CompletedFinished
20192020202120222023202420252026
First PostedSep 7, 2018
Enrollment StartJan 2, 2019
Primary CompletionJan 17, 2023
TodayJul 2, 2026
Enrollment to primary: 4.0 yearsPosted 7.8 years ago

Interventions

Rifampicindrug

Rifampicin will be given in the same way to arms 2, 3 and 4 (weight dependent). Only the strategy of whom to offer PEP differs between the arms.