Subarachnoid Hemorrhage Clinical Trial
Official title:
Clinical Efficacy of In-situ Thrombolysis in Case of Intraventricular Haemorraghia by Aneurysm Rupture
The purpose of this study is to determine the impact of in situ fibrinolysis on the mortality at 30 days in case of subarachnoid hemorrhage.
| Status | Completed |
| Enrollment | 19 |
| Est. completion date | December 2009 |
| Est. primary completion date | December 2009 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - subarachnoid hemorrhage by aneurysm rupture - severe intraventricular hemorraghia Exclusion Criteria: - pregnant women - hemostasis disturbance |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| France | Neurosurgery department , Nice University Hospital | Nice |
| Lead Sponsor | Collaborator |
|---|---|
| Centre Hospitalier Universitaire de Nice |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | assessment of mortality | at 30 days | Yes | |
| Secondary | assessment of morbidity | at 6 months | Yes |
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|---|---|---|---|
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