Comparison of the two treatment modalities (crystallized phenol application vs. surgical treatment) for pilonidal sinus disease

Phase 4

Recruiting

• Conditions: patients with pilonidal sinus disease; Surgery - Surgical techniques; Infection - Other infectious diseases; Skin - Dermatological conditions

• Registration Number: ACTRN12612000868886
• Lead Sponsor: Kamil Gulpinar

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-08-16
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

patients with pilonidal sinus disease

Exclusion Criteria

patients with acute abcess

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
quality of life after treatment[Assessed before the procedure, first day after the procedure and three weeks after the procedure with SF36 and NHP questionnaires]

Secondary Outcome Measures

Name	Time	Method
Pain[Assessed wit VAS at;<br>the first hour after the procedure<br>at 12th, 24th and 48th hour after the procedure<br>and at the 1st week after the procedure]