search
Back to results

Rifaximin Versus Placebo in the Prevention of Travelers' Diarrhea

Primary Purpose

Diarrhea

Status
Completed
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
rifaximin
Sponsored by
DuPont, Hurbert L., MD
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diarrhea focused on measuring Travelers' diarrhea, rifaximin, prophylaxis, enterotoxigenic E. coli

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: An Investigational Review Board approved, written informed consent is appropriately witnessed, signed and dated prior to any study-related activities Male or female subjects 18 years of age or older Able to read and understand English Enrolled and started on prophylaxis within 72 hours of arrival in Mexico If the subject is female, only women with non-childbearing potential or those who are not pregnant will be eligible. Urine pregnancy tests will be performed on those women who question their pregnancy status. Women on the study are required to employ a reliable method of contraception while taking medication. Forms of acceptable contraception include: Double barrier method of contraception. Oral birth control pills for at least two cycles before enrollment and continuing during therapy - subjects will be told they should use a barrier contraception method during the study as well. Norplant inserted at least one month before enrollment. An intrauterine device inserted by a qualified clinician. Medroxyprogesterone acetate for a minimum of one month before study and administered for one month following study completion. An approved birth control patch for at least two cycles before enrollment and continuing during therapy. OR Complete abstinence from intercourse for the two weeks of medication. Exclusion Criteria: Acute diarrhea (criteria for travelers' diarrhea above) within the past week Diarrhea developing within 24 hours of study enrollment In Mexico for more than 72 hours Receipt of one of the following classes of drugs: fluoroquinolone (any drug in class), macrolide or azalide or trimethoprim-sulfamethoxazole within the past week or during the three week study Receipt of other medication to decrease the occurrence of diarrhea (e.g. bismuth subsalicylate or lactobacillus preparations) For females, pregnancy or breast feeding during the three week study Receipt of antidiarrheal medication (loperamide, bismuth subsalicylate, kaopectate) within 24 hours of enrollment Hypersensitivity to rifaximin Unstable medical condition including chronic renal failure and insulin dependent diabetes.

Sites / Locations

  • Universidad Autonoma de Guadalajara

Outcomes

Primary Outcome Measures

Occurrence of diarrhea, defined as passage of >2 unformed stools/24 hr plus one or more signs or symptoms of enteric infection

Secondary Outcome Measures

Occurrence of mild diarrhea (1 or 2 unformed stools/24 hr plus a sign or symptom)
Treatment failure (not well in five days)
Occurrence of moderate to severe abdominal pain/cramps or intestinal gas related symptoms

Full Information

First Posted
December 7, 2004
Last Updated
May 8, 2006
Sponsor
DuPont, Hurbert L., MD
Collaborators
Bausch Health Americas, Inc., The University of Texas Health Science Center, Houston
search

1. Study Identification

Unique Protocol Identification Number
NCT00098384
Brief Title
Rifaximin Versus Placebo in the Prevention of Travelers' Diarrhea
Official Title
A Randomized, Double-Blind, Single Center, Comparative Dose Ranging Study of Rifaximin Vs. Placebo in the Prevention of Travelers' Diarrhea Due to Enteropathogenic Bacteria
Study Type
Interventional

2. Study Status

Record Verification Date
December 2004
Overall Recruitment Status
Completed
Study Start Date
June 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
DuPont, Hurbert L., MD
Collaborators
Bausch Health Americas, Inc., The University of Texas Health Science Center, Houston

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effectiveness of poorly absorbed rifaximin in the prevention of travelers' diarrhea among U.S. college students in Mexico for five weeks.
Detailed Description
This is an investigator-initiated proposal wherein 220 male and female subjects >17 years of age from industrialized regions were randomized to receive a poorly absorbed antibiotic, rifaximin, in one of three doses at mealtime (when they are exposed to diarrhea-causing bacteria), 200 mg once a day, 200 mg twice a day or 200 mg three times a day versus a placebo starting on arrival (within the first 72 hours) to Mexico and continuing for two weeks with diaries of symptoms recorded for three weeks. Adverse events in the subjects were followed for five weeks. If mild diarrhea (1 or 2 unformed stools/24 hours plus an enteric symptom) or diarrheal illness (>2 unformed stools/24 hours plus an enteric symptom) developed, subjects provided a stool sample to determine cause of illness. Forty subjects provided stool samples after 7 days and 14 days treatment to see if their intestinal bacterial flora had developed resistance to rifaximin and to see the level of drug achieved. Stool samples from these forty subjects were studied for enteric pathogens to look for asymptomatic infection during the period of prophylaxis. The stool samples collected were initially processed in our enteric laboratories in Guadalajara, Mexico. Specialized tests such as studies of toxigenicity for enterotoxigenic E. coli and enteroadherence for enteroaggregative E. coli were done in Houston.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea
Keywords
Travelers' diarrhea, rifaximin, prophylaxis, enterotoxigenic E. coli

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
220 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
rifaximin
Primary Outcome Measure Information:
Title
Occurrence of diarrhea, defined as passage of >2 unformed stools/24 hr plus one or more signs or symptoms of enteric infection
Secondary Outcome Measure Information:
Title
Occurrence of mild diarrhea (1 or 2 unformed stools/24 hr plus a sign or symptom)
Title
Treatment failure (not well in five days)
Title
Occurrence of moderate to severe abdominal pain/cramps or intestinal gas related symptoms

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: An Investigational Review Board approved, written informed consent is appropriately witnessed, signed and dated prior to any study-related activities Male or female subjects 18 years of age or older Able to read and understand English Enrolled and started on prophylaxis within 72 hours of arrival in Mexico If the subject is female, only women with non-childbearing potential or those who are not pregnant will be eligible. Urine pregnancy tests will be performed on those women who question their pregnancy status. Women on the study are required to employ a reliable method of contraception while taking medication. Forms of acceptable contraception include: Double barrier method of contraception. Oral birth control pills for at least two cycles before enrollment and continuing during therapy - subjects will be told they should use a barrier contraception method during the study as well. Norplant inserted at least one month before enrollment. An intrauterine device inserted by a qualified clinician. Medroxyprogesterone acetate for a minimum of one month before study and administered for one month following study completion. An approved birth control patch for at least two cycles before enrollment and continuing during therapy. OR Complete abstinence from intercourse for the two weeks of medication. Exclusion Criteria: Acute diarrhea (criteria for travelers' diarrhea above) within the past week Diarrhea developing within 24 hours of study enrollment In Mexico for more than 72 hours Receipt of one of the following classes of drugs: fluoroquinolone (any drug in class), macrolide or azalide or trimethoprim-sulfamethoxazole within the past week or during the three week study Receipt of other medication to decrease the occurrence of diarrhea (e.g. bismuth subsalicylate or lactobacillus preparations) For females, pregnancy or breast feeding during the three week study Receipt of antidiarrheal medication (loperamide, bismuth subsalicylate, kaopectate) within 24 hours of enrollment Hypersensitivity to rifaximin Unstable medical condition including chronic renal failure and insulin dependent diabetes.
Facility Information:
Facility Name
Universidad Autonoma de Guadalajara
City
Guadalajara
State/Province
Jalisco
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
11692292
Citation
DuPont HL, Jiang ZD, Ericsson CD, Adachi JA, Mathewson JJ, DuPont MW, Palazzini E, Riopel LM, Ashley D, Martinez-Sandoval F. Rifaximin versus ciprofloxacin for the treatment of traveler's diarrhea: a randomized, double-blind clinical trial. Clin Infect Dis. 2001 Dec 1;33(11):1807-15. doi: 10.1086/323814. Epub 2001 Oct 23.
Results Reference
background
PubMed Identifier
8502272
Citation
DuPont HL, Ericsson CD. Prevention and treatment of traveler's diarrhea. N Engl J Med. 1993 Jun 24;328(25):1821-7. doi: 10.1056/NEJM199306243282507. No abstract available.
Results Reference
background
PubMed Identifier
15897530
Citation
DuPont HL, Jiang ZD, Okhuysen PC, Ericsson CD, de la Cabada FJ, Ke S, DuPont MW, Martinez-Sandoval F. A randomized, double-blind, placebo-controlled trial of rifaximin to prevent travelers' diarrhea. Ann Intern Med. 2005 May 17;142(10):805-12. doi: 10.7326/0003-4819-142-10-200505170-00005. Erratum In: Ann Intern Med. 2005 Aug 2;143(3):239.
Results Reference
result

Learn more about this trial

Rifaximin Versus Placebo in the Prevention of Travelers' Diarrhea

We'll reach out to this number within 24 hrs