Clinical Trials Directory

Trials / Completed

CompletedNCT00292344

Rifaximin, Loperamide and the Combination to Treat Travelers' Diarrhea

Rifaximin in Standard Three-Day Dosing With and Without the Antimotility Drug, Loperamide, in the Treatment of Travelers' Diarrhea

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
316 (planned)
Sponsor
The University of Texas Health Science Center, Houston · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Most cases of travelers' diarrhea are caused by bacterial pathogens which respond slowly to antibiotic treatment.The study was designed to determine the value of rapidly acting loperamide (imodium) combined with curative dose of the poorly absorbed rifaximin in travelers' diarreha treatment.

Detailed description

During short-term study, adult U.S. students in Mexico (n = 310) with acute diarrhea (≥ 3 unformed stools with enteric symptoms) were enrolled in a double-blind, randomized trial wherein they were given rifaximin 200 mg three times a day for 3 days (R) (n = 102), loperamide 4 mg initially followed by 2 mg after each unformed stool not to exceed 8 mg/day for 2 days (L) (n = 104) or both drugs in the same dosage schedule (L/R) (n = 104). The major outcome parameter was time from initiation of therapy until passage of the last unformed stool before becoming well (TLUS).

Conditions

Interventions

TypeNameDescription
DRUGRifaximin and loperamide

Timeline

Start date
2004-06-01
Completion
2005-08-01
First posted
2006-02-15
Last updated
2009-04-20

Locations

4 sites across 1 country: Mexico

Source: ClinicalTrials.gov record NCT00292344. Inclusion in this directory is not an endorsement.