Loose Seton Prior to Surgery for Single-tract Cryptoglandular Fistula vs no Seton

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorProctos Kliniek

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • No seton placement prior to surgery

    Procedure/Surgery

    No seton placement prior to sfincter preserving surgery

Treatment groups

277 Participants
are divided into 2 treatment groups
Group A: Seton placement prior to surgeryNo intervention 0 interventions
Group B: No seton placement prior to surgeryExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
26 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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