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MicroVention, Inc. Flow Re-Direction Endoluminal Device X (FRED™ X™) Post-Approval Study

Intracranial Aneurysm Clinical Trial

Official title:
MicroVention, Inc. Flow Re-Direction Endoluminal Device X (FRED™ X™) Post-Approval Study

Clinical Trial Summary

The objective of this study is to generate contemporaneous clinical data to facilitate a reasonable comparison of the performance of the FRED™ X™ device with the performance of the FRED™ device. The data generated from this study will be compared to the safety and effectiveness of the FRED™ device by meeting the same performance goals (PGs) established for the FRED™ pivotal study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05409989
Study type Interventional
Source Microvention-Terumo, Inc.
Contact Amy Bowles
Phone 678-858-0992
Email Amy.bowles@microvention.com
Status Recruiting
Phase N/A
Start date September 20, 2022
Completion date November 2029
View Details
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