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NCT Number: NCT02116738

Modified Limberg Procedure Versus Lateral Advancement Flap With Burrow's Triangle Procedure in the Treatment of Pilonidal Sinus

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.

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Key information

Conditions

Sacrococcygeal Pilonidal Disease Cysts Disease Attributes Neoplasms Pathologic Processes Pathological Conditions, Signs and Symptoms Pilonidal Sinus Recurrence

Age range

15 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ankara Mevki Military Hospital : General Surgery Department

Ankara, 06110, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Flap Transposition Procedures

Procedure

Modified Limberg Flap Transposition Procedure and Lateral Advancement Flap Transposition with Burrow's Triangle Procedure in The treatment of Pilonidal Sinus Diseases

Primary outcomes

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

    Time frame: 12 hours

Sponsors and collaborators

Lead sponsor

Ankara Mevki Military Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Apr 17, 2014
Registry last updated
Apr 17, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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