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Single Dose Antibiotic Treatment of Acute Watery Diarrhea, Rifaximin Versus Azithromycin, With Loperamide Adjunct (TrEAT_TD2)

Primary Purpose

Diarrhoea;Acute, Diarrhea Travelers

Status
Recruiting
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Rifaximin 550 MG
Azithromycin 500 MG
Loperamide
Sponsored by
Henry M. Jackson Foundation for the Advancement of Military Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diarrhoea;Acute

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Active duty military, 18-60 years old Presence of acute watery diarrhea (3 or more loose/liquid stools in 24 hours or 2 loose/liquid stools in 24 hours and associated symptoms such as nausea, vomiting, abdominal cramps or tenesmus) lasting <96 hours in duration that impacts function in activities and/or performance of primary duties. Refer to recruitment decision tree below. Eligible for ambulatory management. (Note: Ambulatory management in this study means that the patient can be treated on an outpatient basis to include up to 23 hours of medical observation and IV therapies.) Able to comply with follow-up procedures. Will remain in country for at least 7 days or an assurance that follow-up can be arranged elsewhere. Exclusion Criteria: Allergy to rifamycins, macrolides, or loperamide (not including mild gastrointestinal upset). Antibiotic therapy in the 72 hours prior to presentation (excluding malaria prophylaxis with mefloquine, malarone, chloroquine/proguanil, tafenoquine, or doxycycline). Concomitant medications with known drug-drug interactions with any of the study drugs (includes theophylline, digoxin, warfarin, chloroquine and hydroxychloroquine). Current or history of liver disease or other serious health conditions based on review by study physician. Acute dysentery and/or febrile illness (temperature > 100.4°F [38.1°C]). Presence of symptoms >96 hours prior to initiating treatment. Use of >4 mg loperamide or use of any amount of loperamide for greater than 24 hours prior to enrollment. Prior use of bismuth subsalicylate or other anti-diarrheal, non-antibiotic therapy in the 48 hours prior to enrollment. Positive pregnancy test at presentation (unknown effects with rifaximin). All female participants will be administered a urine pregnancy test prior to enrollment. Previously screened or randomized in this study.

Sites / Locations

  • Camp Lemonnier DjiboutiRecruiting
  • JTF-Bravo, Soto Cano ABRecruiting
  • British Army Training Site UKRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Rifaximin with loperamide

Azithromycin mg with loperamide

Arm Description

Outcomes

Primary Outcome Measures

Therapeutic efficacy of single-dose rifaximin (550 mg) with loperamide in treating acute watery diarrhea compared to single-dose azithromycin (500 mg) with loperamide.
Time to last unformed stool (TLUS), in hours, is calculated from the time of antibiotic dose to last unformed (diarrheal) stool (TLUS).

Secondary Outcome Measures

Proportion of participants no longer meeting TD illness criteria at 24 hours
The clinical efficacy cure rate at 24h is the proportion of participants at the 24h follow up after the initial treatment who met the end point of not meeting TD illness.
Proportion of participants no longer meeting TD illness criteria at 72 hours
For the clinical efficacy cure rate at 72h is the proportions of participants who met the end point no report of unformed/diarrheal/loose/liquid stool (LLS) that meet TD illness >24h after initial treatment and TD-associated symptoms present at 24h were not reported as moderate or greater
Proportion of participants with recurrence of TD illness after previous resolution of TD illness
TD recurrence at 7d follow up if participants meet TD illness and had the previous cure resolution at 24h or 72h
Proportions of serious adverse events (SAE) at 21 days
Proportions of serious adverse events (SAE)

Full Information

First Posted
November 4, 2022
Last Updated
July 6, 2023
Sponsor
Henry M. Jackson Foundation for the Advancement of Military Medicine
Collaborators
Infectious Diseases Clinical Research Program, Uniformed Services University of the Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT05677282
Brief Title
Single Dose Antibiotic Treatment of Acute Watery Diarrhea, Rifaximin Versus Azithromycin, With Loperamide Adjunct
Acronym
TrEAT_TD2
Official Title
A Randomized Controlled Trial Evaluating Single-dose Rifaximin Versus Azithromycin With Loperamide Adjunct for Treatment of Acute Watery Diarrhea
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 28, 2022 (Actual)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Henry M. Jackson Foundation for the Advancement of Military Medicine
Collaborators
Infectious Diseases Clinical Research Program, Uniformed Services University of the Health Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare a single dose of rifaximin with loperamide to the current standard approach of single dose azithromycin with loperamide for the treatment of acute watery traveler's diarrhea (TD). The study requires 1) taking a single dose antibiotic plus loperamide to treat TD, 2) providing blood and stool samples at different time points to evaluate infection and immune responses, 3) completing a daily symptom diary following treatment, 4) being seen by the study doctor to monitor illness and recovery, and 5) completing a brief electronic questionnaire at 3 months. Participants will be randomly assigned to one of the two treatment groups. The two groups are 1) rifaximin 550 mg as a single dose with loperamide 4 mg initially followed by 2 mg after each unformed stool or 2) azithromycin 500 mg as a single dose with loperamide 4 mg initially followed by 2 mg after each unformed stool. Both groups will take the antibiotic dose and 4 mg of loperamide.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhoea;Acute, Diarrhea Travelers

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized, double-blind, active-controlled, treatment trial of Travelers Diarrhea (TD) in an outpatient setting enrolling deployed United States (US) servicemembers assigned to JTF-Bravo, Soto Cano Air Base, Honduras and Camp Lemonnier, Djibouti (CLDJ) and United Kingdom (UK) military personnel to British Army Training Unit, Kenya (BATUK) who present for medical care with acute TD.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rifaximin with loperamide
Arm Type
Experimental
Arm Title
Azithromycin mg with loperamide
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Rifaximin 550 MG
Intervention Description
Rifaximin 550 mg as a single dose administered orally.
Intervention Type
Drug
Intervention Name(s)
Azithromycin 500 MG
Intervention Description
Azithromycin 500 mg as a single dose administered orally.
Intervention Type
Drug
Intervention Name(s)
Loperamide
Intervention Description
4 mg loperamide administered orally with study antibiotic (rifaximin or azithromycin). Additional loperamide to use as needed, but not to exceed 16 mg/day for 2 days as per licensed use (one 2 mg capsule after each looses stool).
Primary Outcome Measure Information:
Title
Therapeutic efficacy of single-dose rifaximin (550 mg) with loperamide in treating acute watery diarrhea compared to single-dose azithromycin (500 mg) with loperamide.
Description
Time to last unformed stool (TLUS), in hours, is calculated from the time of antibiotic dose to last unformed (diarrheal) stool (TLUS).
Time Frame
Up to 1 week (up to 168 hours)
Secondary Outcome Measure Information:
Title
Proportion of participants no longer meeting TD illness criteria at 24 hours
Description
The clinical efficacy cure rate at 24h is the proportion of participants at the 24h follow up after the initial treatment who met the end point of not meeting TD illness.
Time Frame
24 hours
Title
Proportion of participants no longer meeting TD illness criteria at 72 hours
Description
For the clinical efficacy cure rate at 72h is the proportions of participants who met the end point no report of unformed/diarrheal/loose/liquid stool (LLS) that meet TD illness >24h after initial treatment and TD-associated symptoms present at 24h were not reported as moderate or greater
Time Frame
72 hours
Title
Proportion of participants with recurrence of TD illness after previous resolution of TD illness
Description
TD recurrence at 7d follow up if participants meet TD illness and had the previous cure resolution at 24h or 72h
Time Frame
7 days
Title
Proportions of serious adverse events (SAE) at 21 days
Description
Proportions of serious adverse events (SAE)
Time Frame
21 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active duty military, 18-60 years old Presence of acute watery diarrhea (3 or more loose/liquid stools in 24 hours or 2 loose/liquid stools in 24 hours and associated symptoms such as nausea, vomiting, abdominal cramps or tenesmus) lasting <96 hours in duration that impacts function in activities and/or performance of primary duties. Refer to recruitment decision tree below. Eligible for ambulatory management. (Note: Ambulatory management in this study means that the patient can be treated on an outpatient basis to include up to 23 hours of medical observation and IV therapies.) Able to comply with follow-up procedures. Will remain in country for at least 7 days or an assurance that follow-up can be arranged elsewhere. Exclusion Criteria: Allergy to rifamycins, macrolides, or loperamide (not including mild gastrointestinal upset). Antibiotic therapy in the 72 hours prior to presentation (excluding malaria prophylaxis with mefloquine, malarone, chloroquine/proguanil, tafenoquine, or doxycycline). Concomitant medications with known drug-drug interactions with any of the study drugs (includes theophylline, digoxin, warfarin, chloroquine and hydroxychloroquine). Current or history of liver disease or other serious health conditions based on review by study physician. Acute dysentery and/or febrile illness (temperature > 100.4°F [38.1°C]). Presence of symptoms >96 hours prior to initiating treatment. Use of >4 mg loperamide or use of any amount of loperamide for greater than 24 hours prior to enrollment. Prior use of bismuth subsalicylate or other anti-diarrheal, non-antibiotic therapy in the 48 hours prior to enrollment. Positive pregnancy test at presentation (unknown effects with rifaximin). All female participants will be administered a urine pregnancy test prior to enrollment. Previously screened or randomized in this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Principal Investigator
Phone
240-855-6584
Email
contactus@idcrp.org
Facility Information:
Facility Name
Camp Lemonnier Djibouti
City
Djibouti
Country
Djibouti
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Principal Investigator
Phone
2408556584
Email
contactus@idcrp.org
Facility Name
JTF-Bravo, Soto Cano AB
City
Comayagua
Country
Honduras
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Principal Investigator
Phone
2408556584
Email
contactus@idcrp.org
Facility Name
British Army Training Site UK
City
Nanyuki
Country
Kenya
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Principal Investigator
Phone
2408556584
Email
contactus@idcrp.org

12. IPD Sharing Statement

Learn more about this trial

Single Dose Antibiotic Treatment of Acute Watery Diarrhea, Rifaximin Versus Azithromycin, With Loperamide Adjunct

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