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Protocol for Post Marketing Surveillance of Actilyse Vial

Stroke Clinical Trial

Official title:
Protocol for Post Marketing Surveillance of Actilyse Vial

Clinical Trial Summary

The objectives of this study are to review the safety and efficacy of Actilyse Vial (hereafter referred to as "Actilyse") in post-marketing use for treatment of acute ischemic stroke, through investigating followings;

1. Unknown adverse events (especially serious adverse events)

2. Frequency (Incidence) and trend of adverse events under the actual practice

3. Factors on the safety profile of Actilyse

4. Factors on the efficacy profile of Actilyse

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02229799
Study type Observational
Source Boehringer Ingelheim
Contact
Status Terminated
Phase N/A
Start date February 2003
View Details
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