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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01582659
Other study ID # OutCon
Secondary ID
Status Completed
Phase N/A
First received March 27, 2012
Last updated December 4, 2014
Start date June 2012
Est. completion date October 2014

Study information

Verified date December 2014
Source Vejle Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection AgencyDenmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

Constipation is a condition often seen in children. Constipation is often associated with impaired quality of life of the child and of great concern among parents. Despite the fact that both diagnosis and treatment is a simple task, it is often seen that the treatment fails, and many children are referred to a pediatric ward for specialized treatment.

There is currently little research on the subject and treatment is therefore based on expert knowledge rather than scientific research.

The study objective is to identify the most effective and least stressful treatment of children with constipation for both families and the health care system.

The following will be tested:

Does treatment of constipation in children require specialized knowledge and extensive resources or can the treatment be simplified?

The results from this study are expected to form the basis for a evidence based treatment of children with constipation.


Recruitment information / eligibility

Status Completed
Enrollment 239
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers No
Gender Both
Age group 2 Years to 16 Years
Eligibility 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 Hirschsprungs 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.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Telephone counseling
2 planned telephone counseling sessions are conducted.
Web access
Access to a web site with information about childhood constipation similar to the information given at the first visit to the clinic.

Locations

Country Name City State
Denmark Line Modin Kolding
Denmark Pediatric department, Kolding Hospital Kolding

Sponsors (2)

Lead Sponsor Collaborator
Line Modin University of Southern Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Treatment recovery Recovery is defined as the child having no symptoms of constipation according to the Rome III chriteria. 1 year No
Secondary Usage of laxative. Amount of laxative used during the study periode. 1 year No
Secondary Telephone contacts Number of telephone contacts during the study periode, both planned and unplanned contacts will be noted. 1 year No
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