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Evaluation of Platelet Rich Plasma in Skin Graft Take for Patients With Post Burn Raw Areas

Evaluation of Platelet Rich Plasma in Skin Graft Take for Patients With Post Burn Raw Areas

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05996614
Enrollment
40
Registered
2023-08-18
Start date
2023-10-01
Completion date
2025-02-28
Last updated
2023-08-18

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

Conditions

Skin Burn

Brief summary

1. To evaluate the effect of the platelet rich plasma on the take of split thickness skin graft and its early and late results in resurfacing of post burn raw areas. 2. To evaluate the effect of PRP on wound healing on skin graft donor site.

Detailed description

Burn injuries involve tissue destruction due to energy transfer,The burn injuries can be caused by heat from hot liquids, solids or fire, an less common causes are friction, heat, chemical or electric sources The treatment of burns is complex due to the combination of hypermetabolic physiological response and the need for good functional and cosmetic recovery. Split thickness skin grafts (STSGs) are commonly used to resurface large areas of Post burn raw areas. The time to complete wound healing ranged from 2 to 75 days. Factors that significantly affected time to complete wound healing were graft loss by seroma, presence of hypergranulation tissue, premorbid conditions, and total body surface area burned. Generally, skin graft undertakes three steps for healing: anchorage, inosculation, and maturation. Haematoma, shearing, and infection on recipient sites of skin graft can reduce skin graft take, and even lead to skin graft loss. Platelet-rich plasma (PRP) is an autologous blood-derived biomaterial that is enriched with a 2- to 6-fold concentration of platelets in comparison to normal human platelet concentration. Multiple growth factors and bioactive proteins are stored in α-granules of platelets. These growth factors can promote proliferation of endothelial cells, epithelial cells as well as fibroblasts, and increase angiogenesis. The potential clinical application of PRP in skin graft might rely on its haemostasis, adhesive, antibacterial and healing properties.

Interventions

PROCEDUREPRP in skin grafts

topical application of platelet rich plasma before resurfacing with STSG in Post burn raw areas

PROCEDUREconventional methods in skin grafts

fixation of the graft with stitches and staplers

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
15 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age (15- 60 years). 2. Post burn Raw area less than 10 % of total body surface area . 3. Selected donor sites.

Exclusion criteria

1. Raw area due to other causes ( trauma, ischemia,..etc) 2. Patients with bleeding tendency. 3. Patients with comorbidities(diabetes, malignancy,..etc)

Design outcomes

Primary

MeasureTime frameDescription
histopathological biopsy from both groups by punch Biopsy (vancouver scale )3 monthspigmentation (0-2) ,normal 0, Hypopigmentation 1 ,Hyperpigmentation 2 Vascularity (0-3) ,Normal 0, Pink 1, Red 2, Purple 3 Pliability (0-5) Normal 0 ,Supple 1 ,Yielding 2,Firm 3, Banding 4, Contracture 5 Height (0-3) Normal(flat)0 ,(0-2mm)1,(2-5mm)2,(\>5mm)3

Contacts

Primary ContactIbrahim Ragab Ibrahim, master
himo_nimo9@icloud.com00201060865454

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026