116
Participants
Start Date
January 31, 2016
Primary Completion Date
December 31, 2016
Study Completion Date
December 31, 2017
Remifentanil
Subjects in the experimental group will receive remifentanil infusion 0.1-0.4ug/kg/minute before induction of anesthesia and continued until skin closure. During cardiopulmonary bypass, remifentanil infusion will be increased to 0.5-1 ug/kg/min as hemodynamically tolerated.
Fentanyl
Subjects in the control group will initially receive intermittent boluses of Fentanyl in the range of 50-250 ug. Additional fentanyl can be given titrated to hemodynamic parameters throughout surgery.
UPMC Presbyterian Hospital, Pittsburgh
Collaborators (1)
Mylan Inc.
INDUSTRY
Kathirvel Subramaniam
OTHER