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NCT number NCT01801007
Study type Interventional
Source Microvention-Terumo, Inc.
Contact Vinny Podichetty
Phone 7142478043
Status Recruiting
Phase Phase 2/Phase 3
Start date July 2013
Completion date August 2017

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

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

See also
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