Efficacy and Safety of Factor VIIa on Rebleeding After Surgery for Spontaneous Intracerebral Hemorrhage (ICH) (PRE-SICH)
Intracerebral Hemorrhage
About this trial
This is an interventional treatment trial for Intracerebral Hemorrhage focused on measuring Spontaneous intracerebral hemorrhage, ICH, intracerebral rebleeding, cerebral hematoma evacuation, cerebral hematoma volume
Eligibility Criteria
Inclusion Criteria: Male or female, aged 18-75 years inclusive Intraparenchymal primary supratentorial intracerebral hemorrhage requiring surgical evacuation Any Glasgow Coma Score (GCS) score Surgery expected to be performed within 24 hours from symptoms onset Exclusion Criteria: Age below 18 Intraparenchymal hematoma secondary to rupture of cerebral aneurysm or bleeding of arteriovenous (A-V) malformation or cerebral tumors Contemporary involvement in another study Pregnancy Myocardial infarction in the six months preceding enrolment Coronary or carotid stents positioned in the six months preceding enrolment Solid organ transplant patients (e.g., heart, lung, liver, kidney) Pregnancy Myocardial infarction in the six months preceding enrolment Coronary and carotid stents positioned in the six months preceding enrolment Solid organ transplant patients (e.g., heart, lung, liver, kidney)
Sites / Locations
- Azienda Ospedaliera S. Croce e Carle
- Azienda Ospedaliera "Maggiore della Carità"
- II Dpt Anesthesiology&Critical Care Medicine - IRCCS Policlinico S. Matteo
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
1
2
Patients treated with recombinant FVIIa
Patients with spontaneous supratentorial ICH included in this arm will be treated with placebo