drugset / Trial / NCT03864978

Safety and Efficacy of Rifaximin in Patients With Papulopustular Rosacea and Positive Lactulose Breath Test

NCT03864978

Phase 2 Unknown 236 enrolled Alfasigma S.p.A.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Preliminary evidence suggests that treatment with rifaximin may be beneficial in patients with papulopustular rosacea. The present clinical trial is aimed to investigate the safety and efficacy of oral rifaximin delayed release versus placebo in adults with moderate-to-severe papulopustular rosacea (a.k.a. subtype II) and positive lactulose H2/CH4 breath test.

Timeline

Start
2018-06-22
Primary completion
2020-04
Completion
2020-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Rifaximin Other / unclassified 400 mg Oral
Subject Rifaximin Other / unclassified 800 mg Oral

Indications