drugset / Trial / NCT00724126

Rifaximin 3 Times/Day (TID) for Non-Constipation Irritable Bowel Syndrome (IBS)

NCT00724126 ↗

Phase 3 Completed 637 enrolled Bausch Health Americas, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the efficacy of a 14-day course of rifaximin given 3 times a day vs. placebo in providing adequate relief of IBS symptoms.

Timeline

Start
2008-07
Primary completion
2009-08
Completion
2009-09

Outcome

Met primary endpoint

registry NUMBER Placebo: 32.2 percentage of responders NUMBER Rifaximin: 40.6 percentage of responders analysis (unspecified test); Placebo vs Rifaximin; p = 0.03; Regression, Logistic NCT00724126 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Rifaximin Other / unclassified 550 mg —