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Clinical and Fundamental Research on the Combined Use of Escaring and Closed Negative Pressure Wound Therapy

Clinical and Fundamental Research on the Combined Use of Escaring and Closed Negative Pressure Wound Therapy in the Management of Deep Second-Degree Burns

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128763
Enrollment
Unknown
Registered
2026-07-24
Start date
2025-08-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Second-degree burns

Interventions

Negative pressure treatment group after scab ablation:The patient first underwent scab ablation (using a scab grinder to remove necrotic tissue from the wound while preserving the healthy dermis), and
The patient first underwent scab ablation (using a scab grinder to remove necrotic tissue from the wound while preserving the healthy dermis), and immediately after the operation, negative pressure cl

Sponsors

Affiliated Hospital of Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–65 years, no gender restrictions. 2. Confirmed deep second-degree burns covering 5–20% of total body surface area, with 20 subjects per group. 3. Time from injury to admission <=72 hours, with no prior specialised wound treatment (e.g., skin grafting, growth factor application). 4. No severe dysfunction of vital organs (heart, liver, kidneys, etc.), no coagulation disorders, no malignant tumours, and no immunodeficiency diseases. 5. Informed consent obtained from both patient and family members, with signed consent forms.

Exclusion criteria

Exclusion criteria: 1. The wound is complicated with severe infection (such as excessive purulent discharge from the wound, obvious local redness, swelling, heat and pain, and blood routine shows a white blood cell count >15×10^9/L and a neutrophil ratio >85%). 2. People who are allergic to negative pressure treatment materials. 3. Pregnant or lactating women. 4. Those with poor compliance and unable to cooperate to complete the entire treatment cycle and sample collection.

Design outcomes

Primary

MeasureTime frame
Inflammatory indicators of the drainage fluid (tumor necrosis factor -a (TNF-a), interleukin-6 (IL-6), interleukin-10 (IL-10).);

Secondary

MeasureTime frame
Growth factor indicators (vascular endothelial growth factor (VEGF), fibroblast growth factor (bFGF));Matrix metalloproteinases MMPs (MMP-2, MMP-9);Metabolic indicators (total protein, glucose, lactate dehydrogenase, adenosine deaminase);The drainage fluid precipitates the RNA of cells;The effects of VSD drainage fluid on the proliferation, apoptosis and function of fibroblasts and keratinocytes cultured in vitro;Adverse event;

Countries

China

Contacts

Public ContactCheng Jia

Affiliated Hospital of Jiangnan University

doctor_cjwx@sina.com+86 188 6154 7420

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026