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Lactobacillus Reuteri DSM 17938 in the Prevention of Antibiotic-associated Diarrhea in Children: Protocol of a Randomized Controlled Trial

Primary Purpose

Diarrhea, Antibiotic Associated Diarrhea

Status
Completed
Phase
Phase 4
Locations
Poland
Study Type
Interventional
Intervention
Lactobacillus reuteri DSM 17938
Placebo
Sponsored by
Medical University of Warsaw
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diarrhea

Eligibility Criteria

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

Inclusion Criteria:

  • age younger than 18 years;
  • oral or intravenous antibiotic therapy which started within 24 hours of enrollment;
  • signed informed consent.

Exclusion Criteria:

  • pre-existing acute or chronic diarrhea,
  • history of chronic gastrointestinal disease (e.g., inflammatory bowel disease, cystic fibrosis, celiac disease, food allergy) or other severe chronic disease (e.g., neoplastic diseases), immunodeficiency,
  • use of probiotics within 2 weeks prior to enrollment,
  • use of antibiotics within 4 weeks prior to enrollment,
  • prematurity, and exclusive breastfeeding.

Sites / Locations

  • Department of Paediatrics, The Medical University of Warsaw, Poland

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

L reuteri DSM 17938

Controls

Arm Description

L reuteri DSM 17938 2 x 10^8 twice daily

Identically appearing placebo twice daily

Outcomes

Primary Outcome Measures

frequencies of diarrhea and antibiotic associated diarrhea
Three different definitions of diarrhea will be used, as the definitions of diarrhea/AAD in published studies vary. These will include diarrhea defined as: (a) ≥3 loose or watery stools per day for a minimum of 48 hours during antibiotic treatment; (b) ≥3 loose or watery stools per day for a minimum of 24 hours during antibiotic treatment, and (c) ≥2 loose or watery stools per day for a minimum of 24 hours during antibiotic treatment. AAD will be diagnosed in cases of diarrhea, defined clinically as above, caused by C. difficile or for otherwise unexplained diarrhea (i.e., negative laboratory stool tests for infectious agents). In all cases, loose or watery stools will correspond to scores of 5 to 7 on the BSF scale or A-consistency on the AISS.

Secondary Outcome Measures

infectious diarrhea
rotavirus, adenovirus, norovirus, Salmonella, Shigella, Campylobacter, Yersinia and C. difficile
the need for discontinuation of the antibiotic treatment
the need for hospitalization to manage the diarrhea (in outpatients)
the need for intravenous rehydration in any of the study groups
adverse events

Full Information

First Posted
August 16, 2016
Last Updated
March 18, 2018
Sponsor
Medical University of Warsaw
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1. Study Identification

Unique Protocol Identification Number
NCT02871908
Brief Title
Lactobacillus Reuteri DSM 17938 in the Prevention of Antibiotic-associated Diarrhea in Children: Protocol of a Randomized Controlled Trial
Official Title
Lactobacillus Reuteri DSM 17938 in the Prevention of Antibiotic-associated Diarrhea in Children: Protocol of a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
December 2016 (undefined)
Primary Completion Date
March 2018 (Actual)
Study Completion Date
March 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Warsaw

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to assess the effect of Lactobacillus reuteri DSM 17938 administration for the prevention of diarrhea and AAD in children.
Detailed Description
Introduction: Addition of some probiotics appears to reduce the risk of antibiotic-associated diarrhea (AAD). Effects of probiotics are strain specific, thus the efficacy and safety of each probiotic strain should be established separately. We aim to assess the effect of Lactobacillus reuteri DSM 17938 administration for the prevention of diarrhea and AAD in children. Methods and analysis: A total of 250 children younger than 18 years treated with antibiotics will be enrolled into a double-blind, randomized placebo-controlled trial in which they will additionally receive L reuteri DSM 17938 at a dose 2 x 10^8 colony-forming units or an identically appearing placebo, orally, twice daily, for the entire duration of antibiotic treatment. The primary outcome measures will be the frequency of diarrhea and AAD. Diarrhea will be defined according to one of 3 definitions: (a) ≥3 loose or watery stools per day for a minimum of 48 hours during antibiotic treatment; (b) ≥3 loose or watery stools per day for a minimum of 24 hours during antibiotic treatment; (c) ≥2 loose or watery stools per day for a minimum of 24 hours during antibiotic treatment. AAD will be diagnosed in cases of diarrhea, defined clinically as above, caused by C. difficile or for otherwise unexplained diarrhea (i.e. negative laboratory stool tests for infectious agents).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea, Antibiotic Associated Diarrhea

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
L reuteri DSM 17938
Arm Type
Experimental
Arm Description
L reuteri DSM 17938 2 x 10^8 twice daily
Arm Title
Controls
Arm Type
Placebo Comparator
Arm Description
Identically appearing placebo twice daily
Intervention Type
Drug
Intervention Name(s)
Lactobacillus reuteri DSM 17938
Intervention Description
Lactobacillus reuteri DSM 17938 twice daily 2 x 10^8
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
frequencies of diarrhea and antibiotic associated diarrhea
Description
Three different definitions of diarrhea will be used, as the definitions of diarrhea/AAD in published studies vary. These will include diarrhea defined as: (a) ≥3 loose or watery stools per day for a minimum of 48 hours during antibiotic treatment; (b) ≥3 loose or watery stools per day for a minimum of 24 hours during antibiotic treatment, and (c) ≥2 loose or watery stools per day for a minimum of 24 hours during antibiotic treatment. AAD will be diagnosed in cases of diarrhea, defined clinically as above, caused by C. difficile or for otherwise unexplained diarrhea (i.e., negative laboratory stool tests for infectious agents). In all cases, loose or watery stools will correspond to scores of 5 to 7 on the BSF scale or A-consistency on the AISS.
Time Frame
during antibiotic treatment, an average of 10 days and 7 days of follow up
Secondary Outcome Measure Information:
Title
infectious diarrhea
Description
rotavirus, adenovirus, norovirus, Salmonella, Shigella, Campylobacter, Yersinia and C. difficile
Time Frame
during antibiotic treatment, an average of 10 days and 7 days of follow up
Title
the need for discontinuation of the antibiotic treatment
Time Frame
during antibiotic treatment, an average of 10 days
Title
the need for hospitalization to manage the diarrhea (in outpatients)
Time Frame
during antibiotic treatment, an average of 10 days and 7 days of follow up
Title
the need for intravenous rehydration in any of the study groups
Time Frame
during antibiotic treatment, an average of 10 days and 7 days of follow up
Title
adverse events
Time Frame
during antibiotic treatment, an average of 10 days and 7 days of follow up

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age younger than 18 years; oral or intravenous antibiotic therapy which started within 24 hours of enrollment; signed informed consent. Exclusion Criteria: pre-existing acute or chronic diarrhea, history of chronic gastrointestinal disease (e.g., inflammatory bowel disease, cystic fibrosis, celiac disease, food allergy) or other severe chronic disease (e.g., neoplastic diseases), immunodeficiency, use of probiotics within 2 weeks prior to enrollment, use of antibiotics within 4 weeks prior to enrollment, prematurity, and exclusive breastfeeding.
Facility Information:
Facility Name
Department of Paediatrics, The Medical University of Warsaw, Poland
City
Warsaw
ZIP/Postal Code
02-091
Country
Poland

12. IPD Sharing Statement

Citations:
PubMed Identifier
28057659
Citation
Kolodziej M, Szajewska H. Lactobacillus reuteri DSM 17938 in the prevention of antibiotic-associated diarrhoea in children: protocol of a randomised controlled trial. BMJ Open. 2017 Jan 5;7(1):e013928. doi: 10.1136/bmjopen-2016-013928.
Results Reference
derived

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Lactobacillus Reuteri DSM 17938 in the Prevention of Antibiotic-associated Diarrhea in Children: Protocol of a Randomized Controlled Trial

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