50
Participants
Start Date
May 31, 2014
Primary Completion Date
June 30, 2015
Study Completion Date
June 30, 2015
IVIG
Those randomized to the study arm will receive a one time dose of IVIG at 12 our post-Cardiopulmonary bypass. This is significantly early than our current standard of care.
Placebo
If the subject is randomized to the placebo group they will receive a volume of normal saline that is equivalent to the volume of IVIG to be administered based on their weight.
Children's of Alabama, Birmingham
Grifols Biologicals, LLC
INDUSTRY
University of Alabama at Birmingham
OTHER