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A Clinical Study on the Therapeutic Efficacy of Platelet-Rich Plasma Combined with Moist Wound Healing for Pediatric Scald Burns

A Clinical Study on the Therapeutic Efficacy of Platelet-Rich Plasma Combined with Moist Wound Healing for Pediatric Scald Burns

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113185
Enrollment
Unknown
Registered
2025-11-25
Start date
2025-11-30
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Scald

Interventions

Control group:Placebo and moist wound healing
Experimental group:Platelet-rich plasma (PRP) and moist wound healing

Sponsors

Foshan Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The children all suffered burns with an area >=5%, and on the 3rd day after injury, the wound depth was assessed as deep II°; 2. The wound is at the site of the initial injury, without scars, birthmarks, hemangiomas, or other lesions affecting skin color or marks; 3. The children are aged 1-6 years, with no coexisting organ injuries, such as inhalation injuries to the respiratory tract, and no rheumatic autoimmune diseases, skin diseases, nutritional deficiencies, or other conditions; 4. The family accepts the treatment plan, and the children tolerate the treatment.

Exclusion criteria

Exclusion criteria: 1. The wound has clearly met the criteria for skin grafting during the treatment process; 2. During the treatment, it is newly discovered that the patient has a primary skin disease, rheumatic immune disease, or other conditions that are unknown or concealed by the family; 3. During the treatment, the patient develops an allergic reaction to dressings, platelet-rich plasma, etc.; 4. The family does not accept this treatment plan or does not agree to the collection of data by the research group.

Design outcomes

Primary

MeasureTime frame
Hypertrophic scarring;Wound epithelialization time;

Secondary

MeasureTime frame
Total hospitalization cost;Wound infection status.;Hospital stays;Pain assessment;

Countries

China

Contacts

Public ContactYihua Tan

Foshan Maternal and Child Health Hospital

361604474@qq.com+86 757 2297 8125

Outcome results

None listed

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