Overview
In this prospective, randomized trail, duration of non-cutting seton placement in patients with fistula-in-ano is evaluated.
Description
In this prospective, randomized trail, patients are treated in case of fistula-in-ano with non-cutting seton placement. They are then randomized 1:1 in either Group A (duration of placed seton for 4 weeks) or Group B (duration of placed seton for 12 weeks). Patients are participating after informed consent is obtained.
Eligibility
Inclusion Criteria:
- any patient with FIA and treatment with non-cutting seton placement in our institution
- regardless of underlying diagnoses
- age 0-18 years
Exclusion Criteria:
- none