Radiofrequency Treatment for Pilonidal Disease : Safety of Use, Efficacy and Patient Satisfaction at 6 Months (RaTPiD)
Infected Pilonidal Sinus
About this trial
This is an interventional treatment trial for Infected Pilonidal Sinus focused on measuring Radiofrequency
Eligibility Criteria
Inclusion Criteria: patient presenting an infected pilonidal sinus requiring an surgical procedure, at the exception of acute abscess stage Patient aged 18 or above For Women Of Child Bearing Age, use of efficient contraceptive (less than 1% failure) Patient with health insurance coverage French-speaking patient Signed written informed consent Exclusion Criteria: Patient already included in a type 1 interventional research protocol (RIPH1) Patient with cardiac disease (including pacemaker) Patient with skin infection Patient for whom local or general anesthesia is contraindicated patient presenting an anal infectious disease, or an anal fissure or who have previously had a stapled hemorrhoidopexy (Longo procedure) with metallic staples. Patient using anticoagulant or anti-platelet agent (at the exception of aspirin) Patient suffering from innate hemostasis and/or coagulation disorder Patient for whom MRI is contraindicated Pregnant or Breastfeeding women Patient under guardianship or curatorship Patient incarcerated Patient under legal protection Patient refusing follow-up
Sites / Locations
- Groupe Hospitalier Paris Saint-JosephRecruiting
Arms of the Study
Arm 1
Experimental
Radiofrequency
treatment of pilonidal disease according to the Fistura procedure