Clinical Trials Logo

Clinical Trial Summary

The study will compare durations of diarrhea among subjects who report to clinic for treatment and who receive either:

1. standard rifaximin therapy at a dose of 200 mg three times a day for 3 days, OR

2. a single 600 mg dose of rifaximin daily for 3 days.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00875875
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact
Status Withdrawn
Phase Phase 4
Start date June 2009
Completion date June 2009

See also
  Status Clinical Trial Phase
Completed NCT00564863 - Dose-Finding Study of CS19 Expressing ETEC Challenge Strains Phase 1
Completed NCT00564577 - Dose-Finding Study of WS6788A and LSN03-016011/A Enterotoxigenic E. Coli ETEC Challenge Strains That Express CS17 Phase 1
Terminated NCT01005849 - Probiotics and the Prevention of Traveler's Diarrhea Phase 4
Completed NCT00993681 - Travelers' Diarrhea (TD) Vaccine Pivotal Efficacy Study Phase 3
Completed NCT02498301 - Trial Evaluating Chemoprophylaxis Against Travelers' Diarrhea - Prevent TD N/A
Completed NCT00292344 - Rifaximin, Loperamide and the Combination to Treat Travelers' Diarrhea Phase 4
Completed NCT00524004 - Safety and Efficacy of Bovine Milk Immunoglobulin Against CS17 and CsbD Phase 2
Terminated NCT02920242 - A Study Comparing Two Rifaximin Tablets in Patients With Travelers' Diarrhea. Phase 3