Surgical Approach for Pilonidal Disease

Status Completed

Clinical Trial Summary

Clinical Trial Description

In our hospital, between January 2013 and January 2017, those operated with the Modified Limberg flap method after the Rhomboid excision due to pilonidal disease, and those operated with the un-roofing curettage method will be screened retrospectively. Patients who are well followed up will be included in the study. Demographic features will be recorded. Patients will be divided into two groups, the un-roofing curettage group (UC group) and the Modified Limberg Flap group (LF group). Surgery time, hospital stay, return to work time, recovery time, painless walking time, days, painless sitting time in the toilet, days, postoperative VAS, and recurrence will be compared between both groups. In addition, mobilization time, days, recovery time, days, exclusion time, days, wound infection, wound distribution will be compared between groups. The results will be analyzed with the SPSS statistics program. Factors affecting recurrence wound infection, recovery time, hospital stay, operation time, early mobilization will be evaluated by univariate and multivariate logistic regression analysis. ;

Study Design

Related Conditions & MeSH terms

Pilonidal Disease

Clinical Trial Details

NCT number	NCT04334681
Study type	Observational
Source	Konya Meram State Hospital
Contact
Status	Completed
Phase
Start date	April 2, 2020
Completion date	October 1, 2020

View Details

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