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Unroofing Curettage for Pilonidal Disease

Unroofing Curettage for Treating Simple and Complex Sacrococcygeal Pilonidal Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05339828
Enrollment
203
Registered
2022-04-21
Start date
2022-04-27
Completion date
2022-05-05
Last updated
2022-10-27

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

Conditions

Healing Wound, Pilonidal Disease, Recurrence

Keywords

complex pilonidal disease, unroofing curettage, recurrence, Lay open technique

Brief 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.

Interventions

PROCEDUREunroofing curettage

Surgery 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.

Sponsors

Ankara Diskapi Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Consecutive patients aged 18 years or older

Exclusion criteria

* acute pilonidal abscess * poorly controlled * diabetes mellitus, * immunosuppressive or coagulation disorders, * pregnancy and/or lactation, * other acute surgical diseases

Design outcomes

Primary

MeasureTime frameDescription
Recurrence15 daysAfter healing was complete, any new sinus orifice or discharge from the wound was defined as disease recurrence.

Secondary

MeasureTime frameDescription
complete healing time15 daystime after surgery until the wound is completely epithelialized
VAS pain score15 daysVisual analog scale for pain
time to return to daily activities15 daystime after surgery until the to return to daily activities

Countries

Turkey (Türkiye)

Outcome results

None listed

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