Clazosentan in Preventing the Occurrence of Cerebral Vasospasm Following an Aneurysmal Subarachnoid Hemorrhage (aSAH)

PHASE2CompletedINTERVENTIONAL
Enrollment

413

Participants

Timeline

Start Date

January 10, 2005

Primary Completion Date

March 30, 2006

Study Completion Date

March 30, 2006

Conditions
Aneurysmal Subarachnoid Hemorrhage
Interventions
DRUG

Clazosentan 1 mg/h

Subjects receive intravenous clazosentan at a rate of 1 mg/h starting within 56 hours maximum after aneurysm rupture and continuing until Day 14 post-aneurysm rupture

DRUG

Clazosentan 5 mg/h

Subjects receive intravenous clazosentan at a rate of 5 mg/h starting within 56 hours maximum after aneurysm rupture and continuing until Day 14 post-aneurysm rupture

DRUG

Clazosentan 15 mg/h

Subjects receive intravenous clazosentan at a rate of 15 mg/h starting within 56 hours maximum after aneurysm rupture and continuing until Day 14 post-aneurysm rupture

DRUG

Placebo

Subjects receive intravenous placebo starting within 56 hours maximum after aneurysm rupture and continuing until Day 14 post-aneurysm rupture

Trial Locations (16)

Unknown

Dr. Giuseppe Lanzino, Peoria

Dr. Horner, Indianapolis

Dr. Aldrich, Baltimore

Dr. Ogilvy, Boston

Dr. Zuccarello, Cincinnati

Dr. Woo, Cleveland

Dr. Rosenwasser, Philadelphia

Dr. Zager, Philadelphia

Dr. George A. Lopez, Houston

Dr. Bullock, Richmond

Dr. Wong, Calgary

Dr. Findlay, Edmonton

Dr. Redekop, Vancouver

Dr. Ferguson, Toronto

Dr. Bojanowski, Montreal

Dr. Fleetwood, Halifax, Nova Scotia

Sponsors
All Listed Sponsors
lead

Idorsia Pharmaceuticals Ltd.

INDUSTRY