NCT07470294Not yet recruiting
Effectiveness of Different Surgical Techniques for Curative Treatment of Pilonidal Sinus Disease in the Pediatric Population
Effectiveness of Different Surgical Techniques for Curative Treatment of Pilonidal Sinus Disease in the Pediatric Population: A 10-Year Single-Center Retrospective Comparative Cohort Study
Source: ClinicalTrials.gov · Last updated 13 Mar 2026
Brief summary (registry, in English)
Pilonidal sinus disease (PSD) in children is associated with significant morbidity and recurrence risk. Multiple surgical techniques are used, including excision with open healing, primary midline closure, off-midline closure, flap reconstruction, and minimally invasive approaches. However, high-quality comparative data in pediatric populations are limited, and adult data cannot be directly extrapolated. This single-center retrospective cohort study aims to compare the effectiveness of different surgical techniques used for curative treatment of PSD in children treated at CHU Angers between January 1, 2015 and March 31, 2025. The primary endpoint is surgical failure at 2 months, defined as absence of complete wound healing or early recurrence. Secondary outcomes include postoperative complications, time to healing, pain outcomes, length of hospital stay, and recurrence at 1 year. Results are expected to help optimize institutional management strategies and contribute to pediatric-specific evidence.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 90 (estimated)
- First submitted
- 4 Mar 2026
- Start date
- 1 Apr 2026
- Primary completion date
- 31 Aug 2026
- Lead sponsor
- University Hospital, Angers
- NCT number
- NCT07470294
What you commit to
- Study type: Observational
- Planned participants: 90
- From 1 Apr 2026 to the primary completion date, 31 Aug 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Initial surgical management performed at another institution
Other
- Emergency incision and drainage of acute pilonidal abscess (CCAM QBPA001)
- Refusal of participation (patient and/or legal guardians, if applicable)
- Alternative diagnosis (anal abscess, gluteal abscess)
Who the study is looking for
- Age \< 18 years at time of surgery
- Surgical treatment for pilonidal sinus disease
- Surgery performed between January 1, 2015 and March 31, 2025
- Managed at CHU Angers (Pediatric or Visceral Surgery departments)
- ICD-10 diagnosis code L05.9
- CCAM procedure code QBFA007
Age in the registry: 0 years to 18 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.