Viewing Study NCT00412659



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Study NCT ID: NCT00412659
Status: COMPLETED
Last Update Posted: 2016-06-01
First Post: 2006-12-15

Brief Title: Mid-line Excision Versus Karydakis Operation for Pilonidal Sinus
Sponsor: Umeå University
Organization: Umeå University

Study Overview

Official Title: An Expertise-based Randomized Controlled Trial Comparing Midline Excision Versus Karydakis Operation at Surgery for Pilonidal Sinus
Status: COMPLETED
Status Verified Date: 2016-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The trial compares excision in the midline at surgery for pilonidal disease versus excision lateral of the midline Karydakis operation at surgery for pilonidal disease by randomly allocating patients with pilonidal disease to two groups of surgeons each group being trained for one of the two methods
Detailed Description: Excision in the midline and primary suture is a long proven method of treating pilonidal sinus However its associated with high incidence of post operative infection and recurrence On the other hand Karydakis operation excision lateral of the midline transposition flap and primary suture is just a slightly more complicated procedure but has five times less recurrences reported in case series The purpose of the present study is to compare the surgical results and costs of the two surgical methods utilized In addition the investigators aim to compare the quality of life at defined time points after surgery Eligible patients are randomized to two groups of surgeons well trained in either the midline operation or the Karydakis operation expertise based design The design of the study allows wide inclusion criteria for participants a cost-utility approach in the analysis and a high external validity of the conclusions reached

Comparison Midline excision andd primary suture compared with the Karydakis operation excision lateral of the midline and primary suture for pilonidal disease

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None