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Clinical Trial Summary

In this prospective, randomized trail, duration of non-cutting seton placement in patients with fistula-in-ano is evaluated.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05666609
Study type Interventional
Source Friedrich-Alexander-Universität Erlangen-Nürnberg
Contact Sonja Diez, MD
Phone 004991318532923
Email sonja.diez@uk-erlangen.de
Status Recruiting
Phase N/A
Start date January 1, 2023
Completion date December 31, 2027

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