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Clinical Trials/NCT02116738
NCT02116738
Completed
N/A

Interventional Study of the Relatively New Surgical Techniques on the Treatment of Pilonidal Sinus Disease

Ankara Mevki Military Hospital1 site in 1 country1 target enrollmentJune 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Sacrococcygeal Pilonidal Disease
Sponsor
Ankara Mevki Military Hospital
Enrollment
1
Locations
1
Primary Endpoint
Percentage of Participants with a 95% Decrease in Pain Visual Analogue Scale (VAS)
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The investigators want to share our study that is the "Comparison of Modified Limberg Flap Transposition and Lateral Advancement Flap Transposition with Burrow's Triangle in the Surgical Treatment of Sacrococcygeal Pilonidal Sinus.

Detailed Description

Pilonidal Sinus Disease (PSD) is a common and chronic entity of the young adults. So far, many options regarding the surgical treatment of the disease has been described, the consensus about treatment stills remains unsatisfactory, as all the surgical methods have encountered with different rate of recurrences. Our aim in this study is to compare the widely used technique in pilonidal sinus surgical treatment Modified Limberg Flap Transposition and relatively less used technique Lateral Advancement Flap Transposition with Burrow's Triangle, in the terms of VAS scores, recurrence, postoperative complications, surgical site infections in the first 6 months.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
August 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Ankara Mevki Military Hospital
Responsible Party
Principal Investigator
Principal Investigator

MD. Mehmet SAYDAM (General Surgeon)

MD. MEHMET SAYDAM (GENERAL SURGEON)

Ankara Mevki Military Hospital

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of Pilonidal Sinus Disease
  • Must be able to suitable for the surgery

Exclusion Criteria

  • Patients with Recurrent Pilonidal Sinus disease
  • Patient whom is not suitable for surgery

Outcomes

Primary Outcomes

Percentage of Participants with a 95% Decrease in Pain Visual Analogue Scale (VAS)

Time Frame: 12 hours

Study Sites (1)

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