Lactobacillus Reuteri in Children With Constipation
Primary Purpose
Functional Constipation
Status
Unknown status
Phase
Phase 4
Locations
Poland
Study Type
Interventional
Intervention
Lactobacillus reuteri DSM 17938
Placebo
Sponsored by

About this trial
This is an interventional treatment trial for Functional Constipation focused on measuring Probiotics, constipation, children
Eligibility Criteria
Inclusion Criteria:
- Children 3-7 years old
- Occurrence less than three bowel movement per week
- Medical history from at least two months]
- Ineffective laxative treatment at least two months
- The parents approval for child participation in the study and for the treatment
Exclusion Criteria:
- Well-known, organic cause of constipation (i.e. hypothyroidism, Hirschprung disease, cystis fibrosis)
- Anatomic defects of the alimentary canal
- The surgery of the alimentary canal in the past
- Treatment of antibiotics/probiotics during last two weeks before start of the study
Sites / Locations
- ChildrensMHIPolandRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo
Probiotics
Arm Description
Lactobacillus reuteri DSM 17938
Outcomes
Primary Outcome Measures
Number of bowel movement per week, without fecal incontinence
Secondary Outcome Measures
The number of bowel movements per week
Other secondary items are: the number of pain episodes during defecation per week, the number of hard stools, the number of fecal incontinence per week, the number of patients who have to change amount of drug or use of enema.
The number of pain episodes during defecation per week,
The number of hard stools
The number of fecal incontinence per week
The number of patients who have to change amount of drug
The number of patients who have to change use of enema.
Full Information
NCT ID
NCT01388712
First Posted
July 5, 2011
Last Updated
April 1, 2012
Sponsor
Children's Memorial Health Institute, Poland
1. Study Identification
Unique Protocol Identification Number
NCT01388712
Brief Title
Lactobacillus Reuteri in Children With Constipation
Official Title
The Assessment of Lactobacillus Reuteri Efficacy, Provided With Forlax, as Treatment of Incurable Constipation in Children 3-7 Years. Double Blind, Placebo-controlled, Randomized and Multicenter Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Unknown status
Study Start Date
July 2011 (undefined)
Primary Completion Date
April 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Memorial Health Institute, Poland
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The most common cause of children chronic constipation is functional disorders. Functional constipation is diagnosed after excluding organic causes of constipation (anatomical, neurological, endocrinological) and identification of two symptoms defined by the Rome III criteria. There could be low number of bowel movements (below three times a week), defecation pain, fecal incontinence (once a week), stool consistency or occurrence of large diameter stools. The treatment is change of diet, defecation training and application of laxatives.
The probiotics are defined as living microorganisms, which provided in a proper doses should result in beneficial effect on a host health. The assessment of its characteristic is related to strain of bacteria affiliation.
Taking into the consideration that patients with constipation may experience microflora intestine disorders, using the probiotics can have the positive impact on process of treating this disease. The additional reason for using the probiotics during the constipation treatment is an influence of probiotics on movement of the alimentary canal.
In spite of proved effectiveness of some probiotics' strains further research are required, because clinical significance is ambiguous and the effect is confirmed among patients with short medical history. That's way the further analysis of probiotic Lactobacillus reuteri DSM 17938, which was successful treatment method of chronic constipation amongst children (infants) should be performed.
The primary aim of the study is the assessment of Lactobacillus reuteri DSM 17938 efficacy, provided with macrogol (Forlax), as treatment of constipation in 3-7 years old children. The baseline of estimation is the frequency comparison of bowel movement in children belonging into two groups: Lactobacillus reuteri treatment and placebo.
The secondary aim of the study is the assessment of frequency the additional symptoms connected with defecation disorders: such as: number of pain episodes during defecation, the intensity of pain, number of hard stools, number of fecal incontinence per week, number of macrogol (Forlax) pockets used.
The investigators believe that constipation treatment (laxatives- macrogol) with Lactobacillus reuteri has better efficacy that the same treatment without Lactobacillus reuteri in 3-7 years old children with medical history of chronic constipation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Functional Constipation
Keywords
Probiotics, constipation, children
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
128 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Probiotics
Arm Type
Active Comparator
Arm Description
Lactobacillus reuteri DSM 17938
Intervention Type
Dietary Supplement
Intervention Name(s)
Lactobacillus reuteri DSM 17938
Intervention Description
Patients, who met inclusion criteria, will receive following medicaments during 8 weeks: Lactobacillus reuteri DSM 17938 in form of chewing (one tablets containing 10^8CFU).
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Patients, who met inclusion criteria, will receive an identical to probiotic looking and tasting placebo.
Primary Outcome Measure Information:
Title
Number of bowel movement per week, without fecal incontinence
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
The number of bowel movements per week
Description
Other secondary items are: the number of pain episodes during defecation per week, the number of hard stools, the number of fecal incontinence per week, the number of patients who have to change amount of drug or use of enema.
Time Frame
12 weeks
Title
The number of pain episodes during defecation per week,
Time Frame
12 weeks
Title
The number of hard stools
Time Frame
12 weeks
Title
The number of fecal incontinence per week
Time Frame
12 weeks
Title
The number of patients who have to change amount of drug
Time Frame
12 weeks
Title
The number of patients who have to change use of enema.
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
7 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Children 3-7 years old
Occurrence less than three bowel movement per week
Medical history from at least two months]
Ineffective laxative treatment at least two months
The parents approval for child participation in the study and for the treatment
Exclusion Criteria:
Well-known, organic cause of constipation (i.e. hypothyroidism, Hirschprung disease, cystis fibrosis)
Anatomic defects of the alimentary canal
The surgery of the alimentary canal in the past
Treatment of antibiotics/probiotics during last two weeks before start of the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jaroslaw Kierkus, Ph.D.
Phone
+48 228157384
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jaroslaw Kierkus, Ph.D.
Organizational Affiliation
Children's Memorial Health Institute, Poland
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Agnieszka Wegner, M.D.
Organizational Affiliation
Children's Memorial Health Institute, Poland
Official's Role
Principal Investigator
Facility Information:
Facility Name
ChildrensMHIPoland
City
Warsaw
ZIP/Postal Code
04-730
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jaroslaw Kierkus, Ph.D.
Phone
+48 228157384
12. IPD Sharing Statement
Learn more about this trial
Lactobacillus Reuteri in Children With Constipation
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