13
Participants
Start Date
August 17, 2022
Primary Completion Date
June 29, 2024
Study Completion Date
September 29, 2024
Pathogen-Reduced Plasma
The treatment group will receive an additional infusion of Pathogen-Reduced Plasma based on the formula, hourly rate, mL/hr = (1 mL\*kg\*TBSA)/24 hr. This infusion will not be titrated. It will be discontinued at the end of the 24th postburn hour.
Crystalloid Solutions
The control group will receive an additional infusion of LR based on the formula: hourly rate, mL/hr = (1mL\*kg\*TBSA)/24 hr. this infusion will not be titrated. It will be discontinued at the end of the 24th postburn hour.
University of Maryland School of Medicine, Baltimore
University of Alabama at Birmingham Burn Center, Birmingham
Vanderbilt University Medical Center, Nashville
University of Texas Medical Branch, Galveston
U.S. Army Burn Center, Fort Sam Houston
University of Washington School of Medicine, Seattle
Collaborators (1)
Cerus Corporation
INDUSTRY
Coalition for National Trauma Research
OTHER