6
Participants
Start Date
June 30, 2014
Primary Completion Date
January 15, 2017
Study Completion Date
January 15, 2017
Sodium Nitrite
Subjects will receive continuous intravenous infusion of study drug for 7 days at a dose of 64 nmol/min/kg. The infusion will begin shortly after angiographic demonstration of cerebral vasospasm and will be for 7 days unless side effects of the drug dictate stopping the infusion.
University of Virginia Medical Center, Charlottesville
Lead Sponsor
Hope Pharmaceuticals
INDUSTRY