N/A
N=44
Platelet-Rich Plasma (PRP) in Reconstructive Surgery on Children With Retractable Burn Sequelae on Extremities
Burns
Bottom Line
View on ClinicalTrials.gov: NCT00858442 ↗Enrolled (actual)
44
Serious AEs
4.6%
Results posted
Jan 2015
Primary outcome: Primary: Median Time Between Surgery Date and Start Date Compression. — 17; 19 day — p=>0.1574
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- With PRP (Procedure)
- Age
- Pediatric, Adult · 5+ yrs
- Sex
- All
- Sponsor
- Corporation for the Aid of Burned Children
- Primary completion
- Oct 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Median Time Between Surgery Date and Start Date Compression. |
17; 19 | >0.1574 |
| SECONDARY Width of the Graft |
0.1; 0.3 | >0.593 |
| SECONDARY Length of the Graft |
0.2; 0.2 | >0.398 |
Summary
Does the addition of Platelet-Rich Plasma (PRP) to release of burn contractures and skin graft on the limbs of children with retractable burn sequelae reduce the initial time of the compressive treatment and maintain or lower the graft's retraction?
Eligibility Criteria
Inclusion Criteria
- Patients with burn sequelae on their upper or lower limbs
- Treated with release of burn contractures and skin graft on their upper or lower limbs
- Between 5 and 21 years old
- Following instructions in their homes
- With informed and written consent
- Weight 35 Kg or more
- Blood count
- Hepatic and coagulation tests
- Paediatric evaluation prior to surgery
Exclusion Criteria
- Background of blood alterations
- Another current pathology
Data sourced from ClinicalTrials.gov (NCT00858442). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.