Skip to content

Comparison of the results of pilonidal sinus repair with methods of swing flap and secondary intension

Comparison of the results of pilonidal sinus repair with methods of swing flap and secondary intension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210926052604N1
Enrollment
100
Registered
2021-10-21
Start date
2021-10-17
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

Pilonidal sinus. Pilonidal sinus without abscess

Interventions

Intervention 1: Intervention group: Pilonidal sinus repair by swing flap surgery. In this method, the wound repair by displacement of adjacent tissue after removig of pilonidal sinus. Intervention 2:

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Consent to participate in the study Patients referred to Shohada Ashayer Hospital in Khorramabad for pilonidal sinus surgery

Exclusion criteria

Exclusion criteria: Patient with pilonidal sinus abscess Patient with recurrence of the pilonidal sinus Patients with purulent hydroadenitis in the sacrococcygeal region Patient who have risk factors for wound healing (such as iron deficiency anemia, malnutrition, immunodeficiency, diabetes and the use of corticosteroids and anti-metabolic drugs) pregnant women

Design outcomes

Primary

MeasureTime frame
Duration of operation. Timepoint: Operation time. Method of measurement: Time to minutes.;Postoperative site Infection. Timepoint: First week and Second weak after surgery. Method of measurement: Doctor examination.;Hematoma and postoperative bleeding. Timepoint: First week and second week after surgery. Method of measurement: Doctor examination.;Surgery site seroma. Timepoint: 1week and 2week and 1month after surgery. Method of measurement: Doctor examination.;Flap necrosis. Timepoint: 1weak and 2weak after surgery. Method of measurement: Doctor examination.;Recurrence of disease. Timepoint: 3month and 6month after surgery. Method of measurement: Doctor examination.;Interval of recurrence of the disease from the first surgery. Timepoint: 6 month after surgery. Method of measurement: Doctor examination.;Severity of postoperative position pain. Timepoint: 1weak and 2weak and1month and 3month after surgery. Method of measurement: Visual analogue scale questionnaire.;Surgical site scar. Timepoint: 1month and 6month after surgery. Method of measurement: Doctor examination.;Wound dehiscence. Timepoint: 1weak and 2weak and 1month after surgery. Method of measurement: Doctor examination.;Time of wound healing. Timepoint: 3month and 6month after surgery. Method of measurement: Doctor examinatiob.;Return time to daily work. Timepoint: 1 month and 3month after surgery. Method of measurement: Questionnaire.;Postoperative satisfaction. Timepoint: 6month after surgery. Method of measurement: Licrd satisfaction questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed-Ahmad Seyed-Alagheband

Khoram-Abad University of Medical Sciences

Ahmadalagheband@gmail.com+98 66 3330 5006

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026