Skip to content

A Study on Feasibility and effectiveness of using an in situ autologous scar dermal scaffold combined with split-thickness skin for post-burn scar hyperplasia reconstruction.

A Study on Feasibility and effectiveness of using an in situ autologous scar dermal scaffold combined with split-thickness skin for post-burn scar hyperplasia reconstruction.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104813
Enrollment
Unknown
Registered
2025-06-24
Start date
2025-07-03
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Burn scar

Interventions

Observation group (stent group):None
Control group (non stent group):None

Sponsors

The First Affiliated Hospital of the Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 65 Years

Inclusion criteria

Inclusion criteria: Observation group: 1. Meet the diagnostic criteria for post - burn hypertrophic scar; 2. Be treated with autologous scar dermal scaffold combined with split - thickness skin transplantation ; 3. Aged 1 - 65 years old, regardless of gender; 4. Have a post - operative follow - up time of more than six months; 5. Possess complete clinical data and follow - up information. Control group: 1. Meet the diagnostic criteria for post - burn hypertrophic scar; 2. Be treated with intermediate - thickness skin transplantation; 3. Aged 1 - 65 years old, regardless of gender; 4. Have a post - operative follow - up time of more than six months; 5. Possess complete clinical data and follow - up information.

Exclusion criteria

Exclusion criteria: 1. Surgical site infection with ulceration; 2. Severe organ dysfunction; 3. Psychiatric disorders; 4. Lactation or pregnancy; 5. Interrupted follow - up or incomplete clinical data. 6. Metabolic, immune system, or other diseases affecting prognosis.

Design outcomes

Primary

MeasureTime frame
The Patient and Observer Scar Assessment Scale (POSAS) was used to evaluate the scar condition of the recipient area;

Secondary

MeasureTime frame
Scar thickness measured by ultrasound;Skin graft survival rate;Skin elasticity and flexibility;

Countries

China

Contacts

Public ContactHe Ting

The First Affiliated Hospital of the Air Force Medical University

heting2018@fmmu.edu.cn+86 181 9133 6733

Outcome results

None listed

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