Clinical Trials Directory

Trials / Completed

CompletedNCT05339828

Unroofing Curettage for Pilonidal Disease

Unroofing Curettage for Treating Simple and Complex Sacrococcygeal Pilonidal Disease

Status
Completed
Phase
Study type
Observational
Enrollment
203 (actual)
Sponsor
Ankara Diskapi Training and Research Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study aimed to investigate the outcomes of patients who underwent UC as the primary intervention for simple or complex SPD

Detailed description

Sacrococcygeal pilonidal disease (SPD) is a well-known chronic inflammatory condition that affects young adults; There are many treatment options available today, from simple non-surgical methods to extensive flap procedures. However, elaborate treatment strategies can turn this easily treatable disease into a long-term surgical ordeal, causing complications worse than the primary disease itself. While, UC is considered safe and effective for treating simple SPD, its suitability for treating complex disease is poor and controversial. To date, no studies have investigated the efficacy of UC specifically when treating complex SPD. This is the first study to identify and compare efficacy and outcomes after UC in patients classified into simple and complex SPD groups. This study was conducted at the Department of Surgery of the Diskapi Training and Research Hospital in Ankara, Turkey. The local ethics committee of the institution approved the study protocol (number 27/02, dated March 22, 2016), and written informed consent was obtained from all participants.

Conditions

Interventions

TypeNameDescription
PROCEDUREunroofing curettageSurgery was performed with the patient lying in the prone position under local anesthesia. The tract was identified by passing small artery forceps along its length and was then opened by cutting directly down onto the forceps. The sinus and all its tracts were completely unroofed, and the base was curetted to remove all necrotic content, hair, and granulation tissue using a dry gauze. The fibrotic back wall was left as intact as possible to avoid delayed healing. Hemostasis was achieved using diathermy with no drainage needed.

Timeline

Start date
2022-04-27
Primary completion
2022-05-02
Completion
2022-05-05
First posted
2022-04-21
Last updated
2022-10-27

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05339828. Inclusion in this directory is not an endorsement.