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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00823485
Study type Interventional
Source Centre Hospitalier Universitaire de Nice
Contact
Status Completed
Phase Phase 2/Phase 3
Start date October 2005
Completion date December 2009

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