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Optimizing the Management of Acute Diarrhoeal Disease

Primary Purpose

Acute Gastroenteritis

Status
Completed
Phase
Phase 3
Locations
Botswana
Study Type
Interventional
Intervention
Rapid diagnostics
Probiotic
Placebo
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Gastroenteritis focused on measuring diarrhoea, gastroenteritis, rapid diagnostics, probiotics

Eligibility Criteria

2 Months - 60 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • acute diarrhoeal illness (>= 3 stools in 24 hour period)

Exclusion Criteria:

  • diarrhoeal illness >=14 days
  • bloody stool
  • known inflammatory bowel disease, cystic fibrosis, or malignancy
  • live in a household with someone else documented to have a bacterial or parasitic enteric infection of defined aetiology
  • live outside catchment areas
  • no permanent address
  • no access to mobile phone
  • previous participation in this study
  • nosocomial diarrhoea

Sites / Locations

  • Princess Marina Hospital
  • Deborah Retief Hospital
  • Scottish Livingstone Hospital
  • Bamalete Lutheran Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Other

Other

Placebo Comparator

Arm Label

Rapid diagnostics and probiotic

Rapid diagnostics and placebo

No rapid diagnostics and probiotic

No rapid diagnostics and placebo

Arm Description

Participants randomized to this arm will have rapid enteric diagnostics performed on the day of enrolment. Those found to have a treatable pathogen will be prescribed antimicrobials that day. Participants will also be given Lactobacillus reuteri DSM 17938 5 x 10e8 cfu/mL x 60 days.

Participants randomized to this arm will have rapid enteric diagnostics performed on the day of enrolment. Those found to have a treatable pathogen will be prescribed antimicrobials that day. Participants will also be given placebo x 60 days.

Participants randomized to this arm will have stool specimens processed after the conclusion of the study. Participants will also be given Lactobacillus reuteri DSM 17938 5 x 10e8 cfu/mL x 60 days.

Participants randomized to this arm will have stool specimens processed after the conclusion of the study. Participants will also be given placebo x 60 days.

Outcomes

Primary Outcome Measures

Height z-score (HAZ) adjusted for baseline HAZ

Secondary Outcome Measures

Mortality
Weight z-score (WAZ) adjusted for baseline WAZ
Environmental enteropathy score (EES)
composite of stool neopterin, myeloperoxidase, and alpha-1-antitrypsin
Diarrhoea recurrence

Full Information

First Posted
June 14, 2016
Last Updated
February 23, 2019
Sponsor
Hamilton Health Sciences Corporation
Collaborators
Grand Challenges Canada, BioMérieux, BioGaia AB, Copan Italia S.A., Botswana-UPenn Partnership, University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT02803827
Brief Title
Optimizing the Management of Acute Diarrhoeal Disease
Official Title
Optimizing the Management of Pediatric Acute Diarrhoeal Disease in Botswana
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
February 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hamilton Health Sciences Corporation
Collaborators
Grand Challenges Canada, BioMérieux, BioGaia AB, Copan Italia S.A., Botswana-UPenn Partnership, University of British Columbia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Many children admitted to hospital in Botswana without bloody diarrhoea are presumed to have viral gastroenteritis and so not treated with antibiotics - but they may indeed have a treatable cause for their illness. The investigators will conduct a randomized trial to see if rapid testing using novel methods to identify potentially treatable causes of diarrhoea leads to improved outcomes. The investigators will also be randomizing children to Lactobacillus reuteri DSM (daughter strain) 17938 therapy versus placebo (the standard of care) to see if this treatment decreases the duration of diarrhoea. The proposed study is a large multi-centre trial following the previous pilot trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Gastroenteritis
Keywords
diarrhoea, gastroenteritis, rapid diagnostics, probiotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
276 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Rapid diagnostics and probiotic
Arm Type
Experimental
Arm Description
Participants randomized to this arm will have rapid enteric diagnostics performed on the day of enrolment. Those found to have a treatable pathogen will be prescribed antimicrobials that day. Participants will also be given Lactobacillus reuteri DSM 17938 5 x 10e8 cfu/mL x 60 days.
Arm Title
Rapid diagnostics and placebo
Arm Type
Other
Arm Description
Participants randomized to this arm will have rapid enteric diagnostics performed on the day of enrolment. Those found to have a treatable pathogen will be prescribed antimicrobials that day. Participants will also be given placebo x 60 days.
Arm Title
No rapid diagnostics and probiotic
Arm Type
Other
Arm Description
Participants randomized to this arm will have stool specimens processed after the conclusion of the study. Participants will also be given Lactobacillus reuteri DSM 17938 5 x 10e8 cfu/mL x 60 days.
Arm Title
No rapid diagnostics and placebo
Arm Type
Placebo Comparator
Arm Description
Participants randomized to this arm will have stool specimens processed after the conclusion of the study. Participants will also be given placebo x 60 days.
Intervention Type
Other
Intervention Name(s)
Rapid diagnostics
Intervention Description
Participants will have enteric specimens obtained using a flocked rectal swab, which will be transported in 2 mL Cary Blair medium. These will be tested using the BioMerieux BioFire FilmArray GI panel.
Intervention Type
Biological
Intervention Name(s)
Probiotic
Intervention Description
The probiotic given will be Lactobacillus reuteri DSM 17938, 5x10e8 cfu/mL x 60 days, suspended in vegetable oil.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
The placebo will be the vegetable oil vehicle and look identical to the probiotic.
Primary Outcome Measure Information:
Title
Height z-score (HAZ) adjusted for baseline HAZ
Time Frame
60 days post-enrollment
Secondary Outcome Measure Information:
Title
Mortality
Time Frame
60 days post-enrollment
Title
Weight z-score (WAZ) adjusted for baseline WAZ
Time Frame
60 days post-enrollment
Title
Environmental enteropathy score (EES)
Description
composite of stool neopterin, myeloperoxidase, and alpha-1-antitrypsin
Time Frame
60 days
Title
Diarrhoea recurrence
Time Frame
60 days after enrolment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
60 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: acute diarrhoeal illness (>= 3 stools in 24 hour period) Exclusion Criteria: diarrhoeal illness >=14 days bloody stool known inflammatory bowel disease, cystic fibrosis, or malignancy live in a household with someone else documented to have a bacterial or parasitic enteric infection of defined aetiology live outside catchment areas no permanent address no access to mobile phone previous participation in this study nosocomial diarrhoea
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey Pernica, MD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Marina Hospital
City
Gaborone
Country
Botswana
Facility Name
Deborah Retief Hospital
City
Mochudi
Country
Botswana
Facility Name
Scottish Livingstone Hospital
City
Molepolole
Country
Botswana
Facility Name
Bamalete Lutheran Hospital
City
Ramotswa
Country
Botswana

12. IPD Sharing Statement

Citations:
PubMed Identifier
35418412
Citation
Pernica JM, Arscott-Mills T, Steenhoff AP, Mokomane M, Moorad B, Bapabi M, Lechiile K, Mangwegape O, Batisani B, Mawoko N, Muthoga C, Vanniyasingam T, Ewusie J, Lowe A, Bonsu JM, Gezmu AM, Smieja M, Mazhani L, Stordal K, Thabane L, Kelly MS, Goldfarb DM. Optimising the management of childhood acute diarrhoeal disease using a rapid test-and- treat strategy and/or Lactobacillus reuteri DSM 17938: a multicentre, randomised, controlled, factorial trial in Botswana. BMJ Glob Health. 2022 Apr;7(4):e007826. doi: 10.1136/bmjgh-2021-007826.
Results Reference
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Optimizing the Management of Acute Diarrhoeal Disease

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