This is a multi center, phase 2 randomized controlled study to determine the effect of lyophilized plasma in patients on warfarin therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Licensed plasma that has been lyophilized.
Plasma that has been authorized for transfusion.
Assess and Compare Adverse Events
The primary safety objective is to assess the adverse events after infusion of lyophilized plasma compared to control.
Time frame: Duration of Study (Less than or equal to 72 hours)
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