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NOT YET RECRUITING
NCT07701772
NA

LASER VERSUS CRYSTALLIZED PHENOL IN PILONIDAL SINUS DISEASE

Sponsor: Sanliurfa Education and Research Hospital

View on ClinicalTrials.gov

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.

Official title: A PROSPECTIVE RANDOMIZED COMPARISON OF LASER ABLATION AND CRYSTALLIZED PHENOL APPLICATION IN PRIMARY UNCOMPLICATED SACROCOCCYGEAL PILONIDAL SINUS DISEASE

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2026-07-15

Completion Date

2027-03-01

Last Updated

2026-07-14

Healthy Volunteers

No

Interventions

PROCEDURE

Laser Ablation

After a small incision, hair and debris removal, and curettage, laser ablation is performed using a Leonardo Mini 1470 nm diode laser.

PROCEDURE

Crystallized phenol application

After a small incision, hair and debris removal, and curettage, crystallized phenol is applied to the sinus cavity.