Permeaderm Versus Homograft for Full-thickness Burns
Full Thickness Burn
About this trial
This is an interventional treatment trial for Full Thickness Burn focused on measuring PermeaDerm, Cadaver skin, full thickness burn, temporary coverage
Eligibility Criteria
Inclusion Criteria:
- ≥ 2 % total body surface area (TBSA) full thickness burned.
- Patients with two adjacent or body symmetrical full thickness burned areas (each ≥ 1 TBSA) and comparable in size (TBSA ± 0.5), that require debridement and autografting.
Exclusion Criteria:
- Time from injury to admission >= 5 days
- Sepsis on admission or clinically suspected infection (as per attending physician)
- Pregnancy or childbearing
- Positive HIV or hepatitis screens
- History of active malignancy
- Patients who do not require surgical debridement and autografting
- Patient with burn injuries originating from other causes (chemical, and frostbite)
Sites / Locations
- University of texas Medical Branch Galveston
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Active Comparator
Experimental
Active Comparator
Permeaderm as temporary coverage
FHCA as temporary coverage
Permeaderm over widely meshed autograft
FHCA over widely meshed autograft
A: temporary coverage with PermeaDerm until autografting: After randomization of study site, study dressing will be applied as temporary coverage on freshly excised full-thickness burn wounds.
B: temporary coverage with FHCA until autografting: After randomization of study site, study dressing will be applied as temporary coverage on freshly excised full-thickness burn wounds.
C: temporary coverage of widely meshed autograft with PermeaDerm until healing occurs and PermeaDerm can remove
D: temporary coverage of widely meshed autograft with FHCA until healing occurs