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Factors Affecting Wound Dehiscence in Pilonidal Sinus Surgery (ORIPIS)

A

Ankara Etlik City Hospital

Status

Enrolling

Conditions

Pilonidal Sinus Disorder

Treatments

Other: No intervention (observational study)

Study type

Observational

Funder types

Other

Identifiers

NCT07370714
AEŞH-EK-2025-290

Details and patient eligibility

About

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.

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • Patients undergoing emergency surgery
  • Previous pilonidal sinus surgery at the same site
  • Inability to complete postoperative follow-up

Trial design

250 participants in 1 patient group

Pilonidal Sinus Surgery Patients
Description:
This cohort includes adult patients undergoing pilonidal sinus surgery as part of routine clinical care at participating centers. The study is observational in nature, and no experimental intervention is assigned. Surgical technique, anatomical characteristics including proximity to the anal verge, and morphological stage of the disease are determined by the treating surgeon according to standard practice. Patients are prospectively followed after surgery, and postoperative wound outcomes are recorded for observational analysis.
Treatment:
Other: No intervention (observational study)

Trial contacts and locations

1

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Central trial contact

Muhammed Salih Süer, Attendant

Data sourced from clinicaltrials.gov

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