Prospective Database of Factors Associated With Faecal vs. Double Incontinence in Patients Referred for High Resolution Anorectal Manometry.

Recruiting Observational Study
Double Incontinence Faecal Incontinence Urinary Incontinence
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
150 (estimated)
Sponsor
Universitair Ziekenhuis Brussel · Other
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About This Trial
This study aims to verify the results from our previous retrospective cohort analysis by establishing a database of well-characterised patients prospectively. The different prevalence of neurological disorders, abdominal, urological and obstetrical surgery, diarrhoea and other potential associated factors as well as the importance of abnormalities identified by 3D high resolution anorectal manomet…
Trial Locations
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Eligibility 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 …
Contacts

Magali Surmont

+32 2 477 60 11

magali.surmont@uzbrussel.be

CONTACT

Virgini Van Buggenhout

+32 2 477 60 11

virgini.vanbuggenhout@uzbrussel.be

CONTACT