Recombinant Factor VIIa in Acute Intracerebral Haemorrhage
Status: | Completed |
---|---|
Conditions: | Neurology, Hematology |
Therapuetic Areas: | Hematology, Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/13/2017 |
Start Date: | May 2005 |
End Date: | January 2007 |
Randomised, Double-Blind, Placebo Controlled, Multi-Centre, Parallel Groups Confirmatory Efficacy and Safety Trial of Activated Recombinant Factor VII (NovoSeven®/Niastase®) in Acute Intracerebral Haemorrhage
This trial is conducted in Asia, Europe, Middle East, North America, Oceania, and South
America.
The purpose of this study is to evaluate the treatment of Recombinant Factor VIIa (eptacog
alfa (activated)) in patients with acute intracerebral bleeding. It is expected that more
patients will recover without severe permanent disability after acute treatment with
Recombinant Factor VIIa by reducing further intracerebral bleeding.
America.
The purpose of this study is to evaluate the treatment of Recombinant Factor VIIa (eptacog
alfa (activated)) in patients with acute intracerebral bleeding. It is expected that more
patients will recover without severe permanent disability after acute treatment with
Recombinant Factor VIIa by reducing further intracerebral bleeding.
Inclusion Criteria:
- Spontaneous intracranial hemorrhage (ICH) within 3 hours after first symptom
Exclusion Criteria:
- Patients with secondary ICH
- Pre-existing disability
- Haemophilia
We found this trial at
69
sites
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