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Clinical Trial Summary

The purpose of this trial is to investigate safety and efficacy of Cerebrolysin as add-on therapy to standard care in patients with acute traumatic brain injury (TBI). The study duration for each patient is 180 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01606111
Study type Interventional
Source Ever Neuro Pharma GmbH
Contact
Status Terminated
Phase Phase 4
Start date September 2013
Completion date July 2015

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