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Clinical Trial Summary

The purpose of this registry is to assess clinical outcomes, and different factors that may affect these clinical outcomes such as systems of care, associated with the use of Covidien market-released neurothrombectomy devices intended to restore blood flow in patients experiencing acute ischemic stroke due to large intracranial vessel occlusion.


Clinical Trial Description

This is a prospective, multi-center, non-randomized, observational registry of acute ischemic stroke patients that have or will undergo treatment with the use of a Covidien market-released neurothrombectomy device (as the initial device used to remove the thrombus) within 8 hours of stroke symptom onset, at the discretion of the investigator and independent of participation in this registry. This registry may enroll up to 1000 patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02239640
Study type Observational [Patient Registry]
Source Medtronic Neurovascular Clinical Affairs
Contact
Status Completed
Phase
Start date August 21, 2014
Completion date October 7, 2016

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