Pilonidal Cyst Without Abscess

2

Review clinical trials related to Pilonidal Cyst Without Abscess. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Laser Coagulation of Pilonidal Sinus With/Without Intraoperative Ultrasound Control

LASER COAGULATION OF THE PILONIDAL SINUS WITH INTRAOPERATIVE US CONTROL: PROTOCOL FOR A PROSPECTIVE MULTICENTER RANDOMIZED CLINICAL STUDY. Adaptive randomized controlled equivalence study with one planned non-blinded interim analysis.

Participants needed: 310
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: State Scientific Centre of Coloproctology, Russian FederationUpdated: Sep 21, 2026
Eligibility criteria

• chronic inflammation of the pilonidal sinus; [+3]

• acute inflammation (abscess) of the pilonidal sinus; [+2]

Status: Not yet recruiting

SiLaC Laser Technique for Pilonidal Sinus - La Paz Cohort Study.

Pilonidal sinus disease (PSD) is a chronic inflammatory condition of the sacrococcygeal region that frequently affects young adults, often causing pain, drainage, and recurrent infection. Traditional surgical approaches such as wide excision or flap techniques may result in prolonged healing times, relevant postoperative pain, and recurrence rates up to 20-30%. The SiLaC (Sinus Laser-Assisted Closure) technique is a minimally invasive procedure that uses a 1470-nm diode laser fiber to ablate the sinus epithelium and induce concentric contraction of the tract. International studies have reported promising results with faster recovery, minimal wound care, and low morbidity. This prospective single-center cohort study aims to evaluate the clinical outcomes and perceived recovery time of adult patients treated with the SiLaC® technique at Hospital Universitario La Paz (Madrid, Spain). The main outcome is the total recovery time perceived by patients after surgery. Secondary outcomes include postoperative complications, recurrence rate, pain intensity, need for wound care, and patient satisfaction. Data will be collected from medical records and structured follow-up interviews.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Hospital Universitario La PazUpdated: Dec 9, 2025Duration: 6 Months
Eligibility criteria

Age ≥ 18 years. [+3]

Patients with inflammatory bowel disease or complex anorectal fistulas. [+3]