Evaluation of the Recovery Rate and Postoperative Incontinence of Surgical Fistulas in a Cohort of a Reference Centre
NCT ID: NCT03865823
Last Updated: 2025-09-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
600 participants
OBSERVATIONAL
2019-03-01
2026-03-31
Brief Summary
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The proctologist's objective is to treat the infection (anal fistula and abscess) with the minimum impact on anal continence. Drainage of the fistula pathway(s) and removal of infected tissue during initial surgery are essential. The treatment of upper trans-sphincterial fistulas, i. e. those that span more than half the height of the anal sphincter, poses risks to anal continence. It sometimes requires several times of surgical treatment.
The study aim to investigate the fate of all patients treated for anal fistula in an expert team, in terms of impact on healing and anal continence and according to the type of anal fistula, the co-morbidity, the surgical techniques used and the bacterial flora responsible.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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anal Fistula
patient with anal fistula with indication to surgical treatment
pus sample
A pus sample from the fistula will be taken by the doctor during this first consultation or, failing that, in the operating room before disinfection.
Interventions
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pus sample
A pus sample from the fistula will be taken by the doctor during this first consultation or, failing that, in the operating room before disinfection.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Groupe Hospitalier Diaconesses Croix Saint-Simon
OTHER
Responsible Party
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Locations
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Groupe Hospitalier Diaconesses Croix Saint Simon
Paris, , France
Countries
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Other Identifiers
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D_ELK_2018_2
Identifier Type: -
Identifier Source: org_study_id
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