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Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of the MicroVention Flow Redirection Intraluminal Device (FRED) system when used in the treatment of wide-necked intracranial aneurysms.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01801007
Study type Interventional
Source Microvention-Terumo, Inc.
Contact
Status Completed
Phase N/A
Start date July 2013
Completion date January 2018

See also
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