Database of factors related to faecal and double incontinence
Prospective Database of Factors Associated With Faecal vs. Double Incontinence in Patients Referred for High Resolution Anorectal Manometry.
This study is trying to gather information about what causes faecal and double incontinence in people to see how it affects their lives and compare it with those who don’t have these issues.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Universitair Ziekenhuis Brussel Academic / other |
| Locations | 1 site (Brussels, Brussels Capital) |
| Trial ID | NCT05550675 on ClinicalTrials.gov |
What this trial studies
This observational study aims to establish a prospective database to verify previous findings regarding faecal incontinence (FI) and double incontinence (DI) by comparing various associated factors among affected individuals and controls. It will evaluate the prevalence of neurological disorders, surgical history, and other potential risk factors, alongside the impact of these conditions on quality of life. Participants will complete disease-specific questionnaires to assess the severity of their incontinence and its effects on their daily lives. The study will utilize high-resolution anorectal manometry to gather detailed physiological data.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old who self-report experiencing faecal incontinence.
Not a fit: Patients with active rectal inflammation, severe pain, or those unable to complete the required assessments will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of incontinence conditions, leading to improved diagnosis and treatment strategies for affected patients.
How similar studies have performed: Previous studies have indicated potential associations between various factors and incontinence, but this approach using high-resolution manometry is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age \> 18 years; * Self-reported faecal incontinence. Exclusion Criteria: * Impossibility to perform the anorectal manometry because of pain, stenosis or organic disease; * Active (peri)rectal inflammation, including abscess; * Pregnancy; * Inability to cooperate during the anorectal manometry * Impossibility to perform HARM due to pain, stenosis or organic disease; * Inability to complete the questionnaires
Where this trial is running
Brussels, Brussels Capital
- UZ Brussel — Brussels, Brussels Capital, Belgium (Recruiting)
Study contacts
- Study coordinator: Magali Surmont
- Email: magali.surmont@uzbrussel.be
- Phone: +32 2 477 60 11
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.