22
Participants
Start Date
February 9, 2021
Primary Completion Date
August 16, 2021
Study Completion Date
November 30, 2021
Cangrelor
Cangrelor will be used at the FDA recommended dose using a 30 μg/kg bolus followed by 4 μg/kg/min infusion. The duration of cangrelor/placebo infusion will be 2 hours. After completing the first phase of the study, patients will undergo a 1-4 week wash-out period and then will cross-over to the alternative treatment in the second phase
Placebo
Normal saline will be infused for 2 hours. After completing the first phase of the study, patients will undergo a 1-4 week wash-out period and then will cross-over to the alternative treatment in the second phase
University of Florida Jacksonville, Jacksonville
Scott R. MacKenzie Foundation
OTHER
University of Florida
OTHER