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The Use of Lactobacillus Reuteri in Functional Constipation in Children

Primary Purpose

Functional Constipation

Status
Terminated
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
probiotic - Lactobacillus reuteri
placebo - with no active ingredient
Sponsored by
HaEmek Medical Center, Israel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Functional Constipation

Eligibility Criteria

6 Months - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 0.5 - 15 years
  • Diagnosis of functional constipation according to Rome IV criteria

Exclusion Criteria:

  • Children with chronic diseases which could cause constipation: Celiac disease, food allergy, Hypothyroidism, Inflammatory Bowel Disease, electrolytes disturbances, Cystic fibrosis, Hirschsprung disease, Neuropathic conditions (Spinal cord trauma, Neurofibromatosis, Tethered cord) or intestinal pseudo-obstruction.
  • Prematurity (< 34 weeks)
  • S/P intestinal surgery
  • Children treated with medications associated with constipation.
  • Existing malignancy
  • Primary or secondary immunodeficiency

Sites / Locations

  • Emek medical center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Treatment Arm

Placebo Arm

Arm Description

25 consecutive children diagnosed with functional constipation will be treated with full dose PEG (Polyethylene glycol 3350) treatment (dose of ~1g/kg/day) for 12 weeks. After 12 weeks of treatment they will be randomized: treated arm will receive probiotic containing Lactobacillus reuteri for 12 weeks while tapering the PEG dose Dose of 5 drops per day for 48 weeks

25 consecutive children diagnosed with functional constipation will be treated with full dose PEG (Polyethylene glycol 3350) treatment (dose of ~1g/kg/day) for 12 weeks. After 12 weeks of treatment they will be randomized: control arm will receive placebo for 12 weeks while tapering the PEG dose Dose of 5 drops per day for 48 weeks

Outcomes

Primary Outcome Measures

The prevalence of constipation recurrence
according to Rome IV criteria
The prevalence of constipation recurrence
according to Rome IV criteria
failure of maintaining normal bowel movements without PEG and the need to resume PEG treatment
according to Rome IV criteria
failure of maintaining normal bowel movements without PEG and the need to resume PEG treatment
according to Rome IV criteria

Secondary Outcome Measures

The number of bowel movements per week
The investigator will collect the information during the following visits from the patient
The number of episodes of fecal incontinence per week
The investigator will collect the information during the following visits from the patient
The stool consistency in patients without PEG treatment
The investigator will collect the information during the following visits from the patient

Full Information

First Posted
October 10, 2017
Last Updated
October 2, 2018
Sponsor
HaEmek Medical Center, Israel
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1. Study Identification

Unique Protocol Identification Number
NCT03333070
Brief Title
The Use of Lactobacillus Reuteri in Functional Constipation in Children
Official Title
The Use of Lactobacillus Reuteri in Functional Constipation in Children: A Double Blind Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Terminated
Why Stopped
The PI was ended her work in the hospital and no replacement was found.
Study Start Date
June 26, 2018 (Actual)
Primary Completion Date
June 26, 2018 (Actual)
Study Completion Date
June 26, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
HaEmek Medical Center, Israel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Functional constipation (FC) is a common condition in childhood, with an estimated prevalence of 0.7% to 29%.The diagnosis and treatment of FC can be difficult tasks, and children are often referred to specialist services causing treatment to become expensive and time-consuming.The standard treatment based on osmotic laxatives (mainly PEG). The recovery rate is 50% to 60% after 1 year of treatment, with 50% of the children having relapse within 5 years. Studies in adults have established the effectiveness of some lactic acid bacteria in the treatment of chronic constipation.
Detailed Description
Functional constipation (FC) is a common condition in childhood, with an estimated prevalence of 0.7% to 29%.The diagnosis and treatment of FC can be difficult tasks, and children are often referred to specialist services causing treatment to become expensive and time-consuming.The standard treatment based on osmotic laxatives (mainly PEG). The recovery rate is 50% to 60% after 1 year of treatment, with 50% of the children having relapse within 5 years. Studies in adults have established the effectiveness of some lactic acid bacteria in the treatment of chronic constipation.However, it is unclear whether similar effects occur in children. Lactobacilli and Bifidobacteria are the most studied species showing a high safety profile. Both are able to promote colonic peristalsis which could be beneficial for the treatment of constipation .Even though traditional treatment is well established and safe, high proportion of children need prolonged treatment for several months or even years. For many parents there is a concern regarding prolonged treatment with PEG .Lactobacilli, bifidobacteria and FOS (fructooligosaccharide) increase stool frequency and decrease consistency in healthy adults and therefore could prevent recurrence of constipation after PEG withdrawal .The principle investigator hypothesize that treatment with probiotics adjunct to PEG and several months thereafter could decrease the proportion of children needed permanent or prolonged treatment (>12 months) with PEG. The importance of the study and its practical benefits: Treatment with PEG for FC is well established and is considered safe. Despite that, a high proportion of children need prolonged treatment for several months or even years. For many parents there is a concern regarding prolonged treatment with PEG. Previous studies did not demonstrate efficacy of treatment with probiotics or prebiotics in FC. Neither of these studies assessed effectiveness probiotics/prebiotic products as adjunct to the traditional treatment (PEG) of FC in shortening its period. A recently published studies including from Israel, demonstrated efficacy of Lactobacillus reuteri in irritable bowel syndrome, infantile colic and functional abdominal pain .Therefore, demonstration of positive effect of treatment with probiotic product in FC, could imply for potential use of this product in other functional gastrointestinal disorders among children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Functional Constipation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment Arm
Arm Type
Active Comparator
Arm Description
25 consecutive children diagnosed with functional constipation will be treated with full dose PEG (Polyethylene glycol 3350) treatment (dose of ~1g/kg/day) for 12 weeks. After 12 weeks of treatment they will be randomized: treated arm will receive probiotic containing Lactobacillus reuteri for 12 weeks while tapering the PEG dose Dose of 5 drops per day for 48 weeks
Arm Title
Placebo Arm
Arm Type
Placebo Comparator
Arm Description
25 consecutive children diagnosed with functional constipation will be treated with full dose PEG (Polyethylene glycol 3350) treatment (dose of ~1g/kg/day) for 12 weeks. After 12 weeks of treatment they will be randomized: control arm will receive placebo for 12 weeks while tapering the PEG dose Dose of 5 drops per day for 48 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
probiotic - Lactobacillus reuteri
Intervention Description
The treated arm will receive 5 drops per day for 48 weeks
Intervention Type
Other
Intervention Name(s)
placebo - with no active ingredient
Intervention Description
The control arm will receive 5 drops per day for 48 weeks
Primary Outcome Measure Information:
Title
The prevalence of constipation recurrence
Description
according to Rome IV criteria
Time Frame
This measure will be assessed at weeks 24.
Title
The prevalence of constipation recurrence
Description
according to Rome IV criteria
Time Frame
This measure will be assessed at weeks 60.
Title
failure of maintaining normal bowel movements without PEG and the need to resume PEG treatment
Description
according to Rome IV criteria
Time Frame
This measure will be assessed at weeks 24.
Title
failure of maintaining normal bowel movements without PEG and the need to resume PEG treatment
Description
according to Rome IV criteria
Time Frame
This measure will be assessed at weeks 60.
Secondary Outcome Measure Information:
Title
The number of bowel movements per week
Description
The investigator will collect the information during the following visits from the patient
Time Frame
This measure will be assessed at baseline and at 24, 36, 48 and 60 weeks after enrolment
Title
The number of episodes of fecal incontinence per week
Description
The investigator will collect the information during the following visits from the patient
Time Frame
This measure will be assessed at baseline and at 24, 36, 48 and 60 weeks after enrolment
Title
The stool consistency in patients without PEG treatment
Description
The investigator will collect the information during the following visits from the patient
Time Frame
This measure will be assessed at baseline and at 24, 36, 48 and 60 weeks after enrolment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 0.5 - 15 years Diagnosis of functional constipation according to Rome IV criteria Exclusion Criteria: Children with chronic diseases which could cause constipation: Celiac disease, food allergy, Hypothyroidism, Inflammatory Bowel Disease, electrolytes disturbances, Cystic fibrosis, Hirschsprung disease, Neuropathic conditions (Spinal cord trauma, Neurofibromatosis, Tethered cord) or intestinal pseudo-obstruction. Prematurity (< 34 weeks) S/P intestinal surgery Children treated with medications associated with constipation. Existing malignancy Primary or secondary immunodeficiency
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarit Peleg, MD
Organizational Affiliation
Emek Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emek medical center
City
Afula
Country
Israel

12. IPD Sharing Statement

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The Use of Lactobacillus Reuteri in Functional Constipation in Children

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