RES® Prepared With RECELL® Compared to Standard of Care Dressings of Partial-thickness Burns in Ages 1-16 Years

NATerminatedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

March 3, 2020

Primary Completion Date

June 23, 2021

Study Completion Date

June 3, 2022

Conditions
Burns
Interventions
DEVICE

RES (Regenerative Epidermal Suspension) prepared using the RECELL® Autologous Cell Harvesting Device

Application of RES prepared using the RECELL® Autologous Cell Harvesting Device along with Telfa™ Clear primary and Xeroform™ secondary wound dressings.

COMBINATION_PRODUCT

Mepilex® Ag Wound Dressing

Application of Mepilex® Ag Wound Dressing

PROCEDURE

Conventional autografting (only when indicated)

When indicated, conventional autografting in accordance with Investigator's standard practice

Trial Locations (9)

19134

Saint Christopher's Hospital for Children, Philadelphia

23219

Evan Hayes Burn Center, Virginia Commonwealth University, Richmond

27157

Wake Forest Baptist Medical Center, Winston-Salem

29425

Medical University of South Carolina, Charleston

33606

University of South Florida Tampa General Hospital, Tampa

70112

University Medical Center New Orleans, New Orleans

85008

Arizona Burn Center / Valleywise Health, Phoenix

98104

University of Washington Regional Burn Center at Harborview Medical Center, Seattle

27599-7600

University of North Carolina, Chapel Hill

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Biomedical Advanced Research and Development Authority

FED

lead

Avita Medical

INDUSTRY

NCT03626701 - RES® Prepared With RECELL® Compared to Standard of Care Dressings of Partial-thickness Burns in Ages 1-16 Years | Biotech Hunter | Biotech Hunter