Clinical Trial

Factors Affecting Wound Dehiscence in Pilonidal Sinus Surgery (ORIPIS)

Recruiting
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Record status
This record was last updated January 27, 2026 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.
Summary
The goal of this multicenter, prospective, observational study is to investigate factors associated with wound dehiscence following pilonidal sinus surgery. The main questions it aims to answer are: Does the proximity of the pilonidal sinus to the anal verge influence the risk of postoperative wound dehiscence? How do the morphological stage of the disease and the surgical technique used affect wound healing outcomes? Patients undergoing pilonidal sinus surgery as part of routine clinical care will be enrolled prospectively across multiple centers. Clinical, anatomical, and surgical characteristics-including anal proximity, morphological stage, and type of surgical technique-will be recorded. Participants will be followed postoperatively, and wound outcomes will be assessed to identify factors associated with wound dehiscence.
Trial Details
NCT Number NCT07370714
Lead Sponsor Ankara Etlik City Hospital
Conditions Pilonidal Sinus Disorder
Enrollment 250 participants
Start Date 2025-12-01
Primary Completion 2026-06 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-01-27