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Clinical study on the treatment of sacrococcygeal pilose sinus with in situ composite flap contralateral displacement surgery

Sacrococcygeal pilonidal sinus lesions excised from the original incision with arbitrary flap plasty analysis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075436
Enrollment
Unknown
Registered
2023-09-05
Start date
2023-09-20
Completion date
Unknown
Last updated
2023-09-11

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

Conditions

pilonidal sinus

Interventions

Experimental group:Opposite displacement of the composite flap in situ
Control group:Limberg flap

Sponsors

Shijiazhuang People's hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1: Consistent with the clinical manifestations of pilonidal sinus 2: The patients ranged in age from 18 to 60 years 3: Patients can tolerate surgery, and can adhere to treatment 4: Patients are informed about this study and sign a consent form 5. Include those who can follow medical advice and adhere to treatment

Exclusion criteria

Exclusion criteria: 1: Patients with cardiovascular disease or other important organ disease, can not tolerate surgery 2: Pregnant or lactating women or those with mental illness 3: Sacrococcygeal mass not caused by pilonidal sinus 4: Patients with incomplete information

Design outcomes

Primary

MeasureTime frame
Duration of complete wound healing;Postoperative complications;Recurrence;—

Secondary

MeasureTime frame
Pain score;The time of hospitalization;Operative time;Intraoperative bleeding;Postoperative drainage tube removal time;patient satisfaction;—

Countries

China

Contacts

Public ContactGuangyao Dai

Shijiazhuang People's hospital

dgy698@163.com+86 176 0311 6982

Outcome results

None listed

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