Factors Affecting Wound Dehiscence in Pilonidal Sinus Surgery (ORIPIS)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAnkara Etlik City Hospital

About this trial

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.

Eligibility criteria

Qualifiers

Adult patients (≥18 years of age)

Diagnosis of pilonidal sinus disease

Patients undergoing pilonidal sinus surgery as part of routine clinical care

Ability to provide informed consent

Disqualifiers

Patients undergoing emergency surgery

Previous pilonidal sinus surgery at the same site

Inability to complete postoperative follow-up

Trial design

Treatments tested in this trial

  • No intervention (observational study)

Treatment groups

250 Participants
are divided into 1 treatment group

Sponsors and collaborators