90
Participants
Start Date
October 31, 2011
Primary Completion Date
June 30, 2014
Study Completion Date
June 30, 2014
Prostacyclin 1 ng/kg/min
Continuous i.v. infusion of epoprostenol 1 ng/kg/min day 5-10 after SAH
Prostacyclin 2 ng/kg/min
Continuous i.v. infusion of epoprostenol 2 ng/kg/min day 5-10 after SAH
Placebo
Continuous i.v. infusion with placebo day 5-10 after SAH
Rigshospitalet, dep. of neurosurgery, Copenhagen
Rune Rasmussen
OTHER