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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversitair Ziekenhuis Brussel

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 manometry (HARM) will be compared between subjects with feacal incontinence (FI), double incontinence (DI) and controls. Presence and severity of both FI and urinary incontinence (UI) will be evaluated by disease specific questionnaires. Measuring both disease severity and Quality of Life (QoL) is needed to determine the true impact of incontinence. Finally, the impact on quality of life will be compared between both groups.

Eligibility criteria

Qualifiers

Age > 18 years;

Self-reported faecal incontinence.

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Questionnaires

Treatment groups

150 Participants
are divided into 3 treatment groups