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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


Study Design

Related Conditions & MeSH terms

NCT number NCT01801007
Study type Interventional
Source Microvention-Terumo, Inc.
Status Active, not recruiting
Phase Phase 3
Start date July 2013
Completion date December 2017

See also
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