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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02116738
Enrollment
1
Registered
2014-04-17
Start date
2013-06-30
Completion date
2013-08-31
Last updated
2014-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sacrococcygeal Pilonidal Disease

Keywords

flap, pilonidal sinus, vas, recurrence

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.

Interventions

PROCEDUREFlap Transposition Procedures

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

Sponsors

Ankara Mevki Military Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 70 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Percentage of Participants with a 95% Decrease in Pain Visual Analogue Scale (VAS)12 hours

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026