About this trial
Cryptoglandular anal fistulas can cause pain, discharge, recurrent infection, and a prolonged treatment course. In current practice, patients with a single-tract mid-high or high cryptoglandular anal fistula often first undergo placement of a loose seton before definitive sphincter-preserving surgery. Although this staged approach is widely used, high-quality evidence showing that preoperative seton placement improves healing or other patient outcomes is limited.
The SETON trial is a multicenter, randomized, controlled non-inferiority trial that compares two accepted treatment strategies: loose seton placement for approximately 8 weeks followed by definitive sphincter-preserving surgery versus direct sphincter-preserving surgery without prior seton placement. The study aims to determine whether omitting routine seton placement is not inferior in terms of fistula closure 26 weeks after the final surgical intervention.
Secondary outcomes include recurrence, postoperative complications, re-interventions, pain, continence, fistula-related quality of life, generic quality of life, return to work, and healthcare and societal costs. The results of this trial may help determine whether a routinely used treatment step can be safely omitted, potentially reducing treatment burden, shortening the treatment pathway, and lowering costs.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age 18 years or older
Single-tract non-purulent mid-high or high cryptoglandular anal fistula
Eligible for sphincter-preserving surgical treatment
Able to complete Dutch-language questionnaires sent by email
Disqualifiers
Anorectal abscess
Multiple or complex anorectal fistulas
Inflammatory bowel disease or clinical suspicion requiring further investigation
History of anorectal malignancy
Trial design
Parallel
Treatments tested in this trial
No seton placement prior to surgery
Procedure/SurgeryNo seton placement prior to sfincter preserving surgery
Treatment groups
Trial outcomes
Primary outcomes
Fistula healing
Fistula closure is defined as absence of an external opening or discharge on physical examination 26 weeks after the final surgical intervention. In case of clinical uncertainty, closure will be confirmed by magnetic resonance imaging (MRI) or endoanal ultrasound.
Sponsors and contacts
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