Comparing two methods for treating pilonidal cyst abscesses
PILO - Comparison of the Effectiveness of the Simple Puncture Compared to the Incision of an Abscess on the PiLOnidal Sinus
NA · University Hospital, Angers · NCT06378918
This study tests whether a quick puncture method or a traditional cut works better for treating pilonidal cyst abscesses in patients.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 134 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Angers (other gov) |
| Locations | 1 site (Angers) |
| Trial ID | NCT06378918 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of a simple puncture technique versus traditional incision for treating pilonidal cyst abscesses. Patients presenting with abscesses are randomly assigned to receive either treatment under local anesthesia, with antibiotic coverage provided. The study aims to determine which method leads to better healing outcomes and fewer complications. Follow-up assessments are conducted to monitor recovery and any potential recurrence of symptoms.
Who should consider this trial
Good fit: Ideal candidates include adult patients with a pilonidal sinus abscess who require surgical intervention for flattening the abscess.
Not a fit: Patients who have initiated antibiotic therapy prior to consultation, have skin necrosis, or are immunosuppressed may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a less invasive treatment option for patients with pilonidal cyst abscesses, reducing the need for general anesthesia and potentially shortening recovery time.
How similar studies have performed: This approach is novel and has not been previously tested in randomized controlled studies, making it an innovative exploration in the treatment of pilonidal cysts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients with a pilonidal sinus abscess * Surgical indication for flattening the abscess * Recurrent or de novo abscess * Signature of consent to participate in the study Exclusion Criteria: * Antibiotic therapy initiated before the emergency room consultation or before the scheduled consultation * Skin necrosis * Immunosuppression (drug-related or pathological) or diabetes * Spontaneous fistulization * Patients who do not speak French * Pregnant and/or breastfeeding women * Patients without social security coverage * Person deprived of liberty by judicial or administrative decision * Person subject to psychiatric care under duress * Person subject to a legal protection measure * Person unable to express consent
Where this trial is running
Angers
- CHU Angers — Angers, France (RECRUITING)
Study contacts
- Principal investigator: Aurélien VENARA, PHD — University Hospital of Angers
- Study coordinator: Aurélien VENARA, PHD
- Email: AuVenara@chu-angers.fr
- Phone: (0)2 41 35 35 25
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Pilonidal Cyst, abcess, puncture, incision, intergluteal groove