Safety and Efficacy Analysis of FRED® Embolic Device in Aneurysm Treatment
NCT02921698 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2018-05-17
Summary
A prospective, multicenter, observational evaluation of the safety and efficacy of the FRED® device in the treatment of intracranial aneurysms.
Conditions
- Intracranial Aneurysms
Interventions
- DEVICE
-
FRED®
Flow Re-Direction Endoluminal Device
Sponsors & Collaborators
-
Microvention-Terumo, Inc.
lead INDUSTRY
Principal Investigators
-
Laurent Pierot, Prof. · CHU Reims; Reims, France
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-07-31
- Primary Completion
- 2017-02-28
- Completion
- 2017-12-31
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