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Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess The Efficacy and Safety of Three Different Doses (275, 550 AND 1100 MG) of Rifaximin Administered BID For Either Two or Four Weeks in The Treatment of Patients With Diarrhea-Associated Irritable Bowel Syndrome
Conditions
Interventions
Rifaximin
Locations
67
United States
Mayo Clinic Scottsdale
Scottsdale, Arizona, United States
Premeire Pharmaceutical Research
Tempe, Arizona, United States
Advanced Clinical Research Institute
Anaheim, California, United States
Lovelace Scientific Resources
Irvine, California, United States
West Gastroenterology Medical Group
Los Angeles, California, United States
Beverly Hills Gastroenterology
Los Angeles, California, United States
Start Date
December 1, 2005
Primary Completion Date
August 1, 2007
Completion Date
September 1, 2008
Last Updated
November 25, 2019
NCT07481422
NCT05740319
NCT07089420
NCT06866106
NCT05293769
NCT03823742
Lead Sponsor
Bausch Health Americas, Inc.
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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