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Clinical Trials/NL-OMON34690
NL-OMON34690
Not yet recruiting
Not Applicable

Altered brain processing of rectal sensation in children with functional fecal incontinence. - fMRI and rectal barostat

Academisch Medisch Centrum0 sites10 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
functional constipation and fecal incontinence
Sponsor
Academisch Medisch Centrum
Enrollment
10
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • Adolescents between 12\-18 years old who suffer from fecal incontinence for at least 2 years and who fulfill the ROME III criteria for functional constipation or functional non\-retentive fecal incontinence will be eligible for enrolment.;Functional constipation is defined by at least 2 of the following criteria: 1\) spontaneous defecation frequency \<3 per week, 2\) fecal incontinence episodes \*1 per week, 3\) retentive posturing, 4\) painful or hard bowel movements, 5\) passage of large diameter stools and 6\) presence of large fecal mass in the rectum. ;Functional non\-retentive fecal incontinence (FNRFI) is defined by all of the following criteria: 1\) defecation into places inappropriate to the social context at least once per month, 2\) no evidence of an inflammatory, anatomic, metabolic, or neoplastic process that explains the subject\*s symptoms, 3\) no evidence of fecal retention.
  • All study subjects and/or the parents should sign informed consent before enrolment.

Exclusion Criteria

  • Patients with 1\) organic causes of constipation, including Hirschsprung\*s disease, muscle disorders, prior recto\-anal surgery, spina bifida, mental retardation or hypothyroidism, 2\) intercurrent illness or active colitis, 3\) known allergy to latex or polyethylene, 4\) incapable to verbally cooperate or 5\) claustrophobia will be excluded from the study.

Outcomes

Primary Outcomes

Not specified

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