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Clinical application and effect analysis of Zunyi's Suture Method in closing anterolateral thigh flap donor area tension incision

Clinical application and effect analysis of Zunyi's Suture Method in closing anterolateral thigh flap donor area tension incision

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045874
Enrollment
Unknown
Registered
2021-04-25
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

scar

Interventions

“Zunyi's Suture Method" group:The anterofemoral tension incision was sutured with Zunyi's Suture Method
Traditional suture group:The anterofemoral tension incision was sutured using a traditional suture method

Sponsors

Department of Burns and Plastic Surgery, Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 55 years, no gender limit; 2. No disease symptoms that affect the healing of surgical incisions, such as scurvy, osteogenesis imperfecta, Ehlers-Danlos syndrome, scar constitution, etc.; 3. No serious heart, liver, kidney, and blood system and other important organ diseases; 4. Patients who are able to give their informed consent and are willing to return for follow-up within 3 months; 5. Preserving the fascia lata during the operation; 6. Thickness of subcutaneous fat on the anterolateral thigh: 1cm-5cm; 7. Cut the range of the anterolateral rotatory thigh donor valve area; 8. Cut width: The ratio of the maximum width of the wound at the donor site of the anterolateral descending branch flap to the circumference of the thigh is less than 16%; 9. Incision tension > 0 Newton (N).

Exclusion criteria

Exclusion criteria: 1. There is a need for long-term outdoor work; 2. Patients who are allergic or intolerant to the sutures and drugs used; 3. Participated in other clinical trials in the last 3 months; 4. Any medical history, according to the researcher's judgment, may interfere with the results of the experiment or increase the patient's risk; 5. The researcher judged that the compliance was not good and the plan could not be strictly implemented.

Design outcomes

Primary

MeasureTime frame
Patient and Observer Scar Assessment Scale (POSAS) Score;

Secondary

MeasureTime frame
Wound complications;

Countries

China

Contacts

Public ContactHe Guijia

Affiliated Hospital of Zunyi Medical University

914260656@qq.com+86 18980592677

Outcome results

None listed

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