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Azithromycin, With or Without Loperamide, to Treat Travelers' Diarrhea

Primary Purpose

Diarrhea

Status
Completed
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Azithromycin 500 mg
Azithromycin 1000 mg
Loperamide
Placebo
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diarrhea focused on measuring Diarrhea, Travel, Travelers' diarrhea, Azithromycin, Loperamide, Treatment, Antibiotic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Eligible subjects included men or women, recently arrived in Mexico, at least 18 years of age, who developed acute diarrhea, which was defined as passage of 3 or more unformed stools in the preceding 24 hours accompanied by one or more signs or symptoms of enteric infection (e.g., nausea, vomiting, abdominal cramps, tenesmus, passage of grossly bloody stools or fecal urgency) with a duration of illness of less than or equal to 72 hours. Exclusion Criteria: Exclusion criteria included pregnancy, breast feeding, an unstable medical condition, taking two or more doses of an antidiarrheal medication in the 24 hours before enrollment or any number of doses of symptomatic therapy within 2 hours of enrollment, or receiving an antimicrobial drug with expected activity against enteric bacterial pathogens within 7 days prior to enrollment.

Sites / Locations

  • University of Texas Enteric Disease Research Clinics

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Experimental

Arm Label

Azithromycin 500 mg plus Placebo

Azithromycin 1000 mg plus Placebo

Azithromycin 500 mg plus Loperamide

Arm Description

a single 500 mg dose of Azitrhomycin at the start of treatment; a single loading dose of placebo at the start of treatment and then a dose of placebo after each loose stool

a single 1000 mg dose of Azitrhomycin at the start of treatment; a single loading dose of placebo at the start of treatment and then a dose of placebo after each loose stool

a single 500 mg dose of Azitrhomycin at the start of treatment; a single 4 mg loading dose of Loperamide at the start of treatment and then 2 mg Loperamide after each loose stool

Outcomes

Primary Outcome Measures

Hours from beginning treatment to passage of last unformed stool

Secondary Outcome Measures

Number of unformed stools passed per 24 hour period
Number of subjects with symptoms of enteric disease per 24 hour period
Symptoms of enteric disease include nausea, vomiting, abdominal cramps, gas, urgency, and tenesmus.
Number of treatment failures
Treatment failure is defined as persisting ill after 72 hours
Percent of subjects in whom enteropathogen isolated from an enrollment stool sample was eradicated from a day 5 stool
Percent of subjects continuing to pass 3 or more (enrollment criteria) unformed stools in a 24 hour period

Full Information

First Posted
August 1, 2006
Last Updated
June 17, 2015
Sponsor
The University of Texas Health Science Center, Houston
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1. Study Identification

Unique Protocol Identification Number
NCT00359970
Brief Title
Azithromycin, With or Without Loperamide, to Treat Travelers' Diarrhea
Official Title
Loperamide Plus Azithromycin More Effectively Treats Travelers' Diarrhea In Mexico Than Azithromycin Alone
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
June 2002 (undefined)
Primary Completion Date
August 2003 (Actual)
Study Completion Date
August 2003 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In a previous study azithromycin proved as efficacious as levofloxacin in the treatment of travelers' diarrhea in Mexico. Because the addition of loperamide to some antibiotics (e.g., trimethoprim-sulfamethoxazole and ofloxacin) has proven more efficacious than antibiotic alone in the treatment of travelers' diarrhea, we decided to study the addition of loperamide to azithromycin. US adults with acute diarrhea in Guadalajara Mexico were randomized to receive azithromycin in two different doses or loperamide plus azithromycin. The duration of diarrhea was shorter (11 hours) in the combination-treated group compared to the antibiotic-treated groups (34 hours). The percentage of subjects continuing to pass 6 or more unformed stools in the first 24 hours was less (1.7%) in the combination-treated group than in the antibiotic-treated groups (20%). We feel loperamide should routinely be added to an antibiotic to optimize treatment of travelers' diarrhea.
Detailed Description
Background. The combination of loperamide and trimethoprim-sulfamethoxazole or a fluoroquinolone has proven to be more efficacious than the antimicrobial agent alone in the treatment of travelers' diarrhea. We set out to prove loperamide plus azithromycin was more efficacious that azithromycin alone. Methods. During the summers of 2002-3, 176 US adults recently arrived in Guadalajara, Mexico were enrolled in a prospective, double-blinded, randomized trial of the treatment of acute diarrhea. Subjects received single doses (1000 mg or 500 mg) of azithromycin or a single 500 mg dose of azithromycin plus loperamide. Subjects gave a pre and post treatment stool sample for analysis and maintained daily diaries of symptoms and passage of stools. Results. The MIC90 of azithromycin for all E. coli and Shigella was 0.03 and 4 µg/ml with eradication rates in day 5 stools of 88% and 100%, respectively. The duration of diarrhea was significantly (p=0.0002) shorter following treatment with azithromycin plus loperamide (11 h) than with either dose of azithromycin alone (34 h). In the first 24 h the average number of unformed stools passed was 3.4 (azithromycin-alone) and 1.2 (combination) for a significant (p<0.0001) difference of 2.2 unformed stools. This difference equated with 20% of azithromycin-treated subjects continuing to pass 6 or more unformed stools in the first 24 h post treatment compared with only 1.7% of combination-treated subjects. Conclusions. For the treatment of travelers' diarrhea in an E. coli predominant region of the world a single 500 mg dose of azithromycin appeared as effective as a 1000 mg dose. Loperamide plus 500 mg azithromycin was safe and more effective than either dose of azithromycin. To realize the substantial clinical benefit that accrues to a subset of subjects, we feel loperamide should routinely be used in combination with an antimicrobial agent to treat travelers' diarrhea.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea
Keywords
Diarrhea, Travel, Travelers' diarrhea, Azithromycin, Loperamide, Treatment, Antibiotic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
176 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Azithromycin 500 mg plus Placebo
Arm Type
Active Comparator
Arm Description
a single 500 mg dose of Azitrhomycin at the start of treatment; a single loading dose of placebo at the start of treatment and then a dose of placebo after each loose stool
Arm Title
Azithromycin 1000 mg plus Placebo
Arm Type
Active Comparator
Arm Description
a single 1000 mg dose of Azitrhomycin at the start of treatment; a single loading dose of placebo at the start of treatment and then a dose of placebo after each loose stool
Arm Title
Azithromycin 500 mg plus Loperamide
Arm Type
Experimental
Arm Description
a single 500 mg dose of Azitrhomycin at the start of treatment; a single 4 mg loading dose of Loperamide at the start of treatment and then 2 mg Loperamide after each loose stool
Intervention Type
Drug
Intervention Name(s)
Azithromycin 500 mg
Other Intervention Name(s)
Zithromax, Zmax
Intervention Description
A single 500 mg dose at the start of treatment
Intervention Type
Drug
Intervention Name(s)
Azithromycin 1000 mg
Other Intervention Name(s)
Zithromax, Zmax
Intervention Description
A single 1000 mg dose at the start of treatment
Intervention Type
Drug
Intervention Name(s)
Loperamide
Other Intervention Name(s)
IModium, Loperamide HCl
Intervention Description
A single 4 mg loading dose at the start of treatment and then 2 mg after each loose stool
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
A single loading dose at the start of treatment and then a dose after each loose stool
Primary Outcome Measure Information:
Title
Hours from beginning treatment to passage of last unformed stool
Time Frame
subjects recorded the time and form of all stools passed during a 4 day observation period
Secondary Outcome Measure Information:
Title
Number of unformed stools passed per 24 hour period
Time Frame
24 hours after treatment
Title
Number of subjects with symptoms of enteric disease per 24 hour period
Description
Symptoms of enteric disease include nausea, vomiting, abdominal cramps, gas, urgency, and tenesmus.
Time Frame
24 hours after treatment
Title
Number of treatment failures
Description
Treatment failure is defined as persisting ill after 72 hours
Time Frame
72 hours after treatment
Title
Percent of subjects in whom enteropathogen isolated from an enrollment stool sample was eradicated from a day 5 stool
Time Frame
5 days after treatment
Title
Percent of subjects continuing to pass 3 or more (enrollment criteria) unformed stools in a 24 hour period
Time Frame
24 hours after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Eligible subjects included men or women, recently arrived in Mexico, at least 18 years of age, who developed acute diarrhea, which was defined as passage of 3 or more unformed stools in the preceding 24 hours accompanied by one or more signs or symptoms of enteric infection (e.g., nausea, vomiting, abdominal cramps, tenesmus, passage of grossly bloody stools or fecal urgency) with a duration of illness of less than or equal to 72 hours. Exclusion Criteria: Exclusion criteria included pregnancy, breast feeding, an unstable medical condition, taking two or more doses of an antidiarrheal medication in the 24 hours before enrollment or any number of doses of symptomatic therapy within 2 hours of enrollment, or receiving an antimicrobial drug with expected activity against enteric bacterial pathogens within 7 days prior to enrollment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles D. Ericsson, MD
Organizational Affiliation
University of Texas Medical School at Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas Enteric Disease Research Clinics
City
Guadalajara
State/Province
Jalisco
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
14557959
Citation
Adachi JA, Ericsson CD, Jiang ZD, DuPont MW, Martinez-Sandoval F, Knirsch C, DuPont HL. Azithromycin found to be comparable to levofloxacin for the treatment of US travelers with acute diarrhea acquired in Mexico. Clin Infect Dis. 2003 Nov 1;37(9):1165-71. doi: 10.1086/378746. Epub 2003 Sep 30.
Results Reference
background
PubMed Identifier
17883462
Citation
Ericsson CD, DuPont HL, Okhuysen PC, Jiang ZD, DuPont MW. Loperamide plus azithromycin more effectively treats travelers' diarrhea in Mexico than azithromycin alone. J Travel Med. 2007 Sep-Oct;14(5):312-9. doi: 10.1111/j.1708-8305.2007.00144.x.
Results Reference
background

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Azithromycin, With or Without Loperamide, to Treat Travelers' Diarrhea

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