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Maintenance Treatment for Children With Constipation

Primary Purpose

Constipation

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Polyethylene glycol 3350
Placebo
Sponsored by
Line Modin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Constipation focused on measuring Constipation, Maintenance treatment, Ultrasound of rectum

Eligibility Criteria

2 Years - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children between 2 and 16 years and referral to our out patient clinic with either constipation or fecal incontinence.
  • Patients must fulfill the Rome III criteria of constipation, which mean they must have at least 2 of the following characteristics: fewer than 3 bowel movements weekly, more than 1 episode of fecal incontinence weekly, large stools in the rectum by digital rectal examination or palpable on abdominal examination, occasional passing of large stools, display of retentive posturing and withholding behavior, and painful defecation.

Exclusion Criteria:

  • Children with known organic causes of constipation, including Hirsprung disease, spinal and anal congenital abnormalities, previous surgery on the colon, inflammatory bowel disease, allergy and metabolic or endocrine diseases.
  • Children receiving drugs known to affect bowel function during a 2 month period before initiation.
  • The healthy control group consists of children with no history of constipation (Rome III), urinary incontinence, urinary tract infections, fecal incontinence, laxative use or any other disease affecting the digestive system.
  • Children receiving medications known to affect bowel function are excluded from the study.

Sites / Locations

  • Line Modin

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Active maintenance treatment

Placebo maintenance treatment

Arm Description

Outcomes

Primary Outcome Measures

Treatment Recovery
Recovery is defined as the child having no symptoms of constipation according to the Rome III criteria.

Secondary Outcome Measures

Usage of Laxative

Full Information

First Posted
March 27, 2012
Last Updated
August 4, 2016
Sponsor
Line Modin
Collaborators
University of Southern Denmark, Kolding Sygehus
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1. Study Identification

Unique Protocol Identification Number
NCT01566409
Brief Title
Maintenance Treatment for Children With Constipation
Official Title
Maintenance Treatment With Polyethylene Glycol 3350 for Children With Constipation. A Randomized, Placebocontrolled Intervention Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
September 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Line Modin
Collaborators
University of Southern Denmark, Kolding Sygehus

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Constipation is a common problem among children. The majority of children suffering from constipation have no underlying disease. Although constipation has no basis in underlying disease, it often leads to a reduced quality of life of children who are on par with or worse than for children suffering from serious diseases such as cardiovascular and rheumatic diseases. Despite the high frequency of constipation among children, little is known about the causes and treatment of constipation. Treatment consists of symptomatic treatment with various laxatives. Movicol and Movicol junior has proven very effective and are therefore widely used in children as disimpaction and maintenance treatment. There is currently no research to prove the need for and length of maintenance treatment with laxative medications in children. The purpose is to examining the effectiveness of maintenance treatment with Movicol. Additional til study will examine how the anal diameter change during a course of treatment and the degree to which it can be used as an indicator of treatment efficacy. The study will test the following: • What is the effect of maintenance treatment with PEG compared to placebo? The results from this study are expected to form the basis for an evidence-based approach to the use of maintenance therapy and the use of ultrasound of the rectum in children with constipation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation
Keywords
Constipation, Maintenance treatment, Ultrasound of rectum

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
115 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active maintenance treatment
Arm Type
Active Comparator
Arm Title
Placebo maintenance treatment
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Polyethylene glycol 3350
Other Intervention Name(s)
Movicol, Movicol junior, Moxalole, Lacrofarm
Intervention Description
Powder for solution. Each sachet contains 13.125 g of macrogol 3350. Disimpaction dosage consists of 1,5 g/kg, maintenance treatment are adjusted according til the Bristol stool chart. The drug can be taken at anytime of the day and can also be divided. Treatment duration up to ½ year.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo will be manufactured and packaged as a powder to make it identical to the bags with the PEG 3350. The powder will comprise of a non-active substance, like a mild rehydration solution, which is a composition consisting of salt and sugar.
Primary Outcome Measure Information:
Title
Treatment Recovery
Description
Recovery is defined as the child having no symptoms of constipation according to the Rome III criteria.
Time Frame
½ year
Secondary Outcome Measure Information:
Title
Usage of Laxative
Time Frame
½ year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children between 2 and 16 years and referral to our out patient clinic with either constipation or fecal incontinence. Patients must fulfill the Rome III criteria of constipation, which mean they must have at least 2 of the following characteristics: fewer than 3 bowel movements weekly, more than 1 episode of fecal incontinence weekly, large stools in the rectum by digital rectal examination or palpable on abdominal examination, occasional passing of large stools, display of retentive posturing and withholding behavior, and painful defecation. Exclusion Criteria: Children with known organic causes of constipation, including Hirsprung disease, spinal and anal congenital abnormalities, previous surgery on the colon, inflammatory bowel disease, allergy and metabolic or endocrine diseases. Children receiving drugs known to affect bowel function during a 2 month period before initiation. The healthy control group consists of children with no history of constipation (Rome III), urinary incontinence, urinary tract infections, fecal incontinence, laxative use or any other disease affecting the digestive system. Children receiving medications known to affect bowel function are excluded from the study.
Facility Information:
Facility Name
Line Modin
City
Kolding
ZIP/Postal Code
6000
Country
Denmark

12. IPD Sharing Statement

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Maintenance Treatment for Children With Constipation

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