Clinical Trial

LASER VERSUS CRYSTALLIZED PHENOL IN PILONIDAL SINUS DISEASE

Study acronym: PSD-L-F
Not Yet Recruiting
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Summary
This single-center prospective randomized parallel-group trial compares laser ablation and crystallized phenol application in adults with primary uncomplicated sacrococcygeal pilonidal sinus disease. The primary objective is to compare postoperative day 1 pain intensity between the two treatment methods. Secondary objectives include complete epithelialization by day 30, time to complete epithelialization, postoperative day 7 pain, duration of analgesic use, time to return to daily activities and work, early local complications, and 6-month recurrence.
Trial Details
NCT Number NCT07701772
Lead Sponsor Sanliurfa Education and Research Hospital
Conditions Sacrococcygeal Pilonidal Sinus Disease, Pilonidal Sinus Disease
Enrollment 120 participants
Start Date 2026-07-15
Primary Completion 2027-03-01 (estimated)
Study Completion 2027-03-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-14