Intravenous Nitrite Infusion for Reversal of Cerebral Vasospasm After Subarachnoid Hemorrhage

PHASE2TerminatedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

June 30, 2014

Primary Completion Date

January 15, 2017

Study Completion Date

January 15, 2017

Conditions
Subarachnoid Hemorrhage
Interventions
DRUG

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.

Trial Locations (1)

22908

University of Virginia Medical Center, Charlottesville

Sponsors
All Listed Sponsors
lead

Hope Pharmaceuticals

INDUSTRY