Travelers' Diarrhea Clinical Trial
Official title:
Single Daily Dose Rifaximin vs. Standard Thrice Daily Dosing for the 3-Day Treatment of Travelers' Diarrhea
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.
n/a
Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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 |