Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate the safety of the Apollo™ Onyx™ Delivery Microcatheter used for delivery of the Onyx™ Liquid Embolic System during brain arteriovenous malformation (AVM) embolization procedures.

Clinical Trial Description

This study is a prospective, single-arm, multicenter, post-market safety evaluation of subjects indicated for embolization of brain AVMs with the study device. The study device was developed to potentially minimize the side effects of catheter retainment and increased procedural risk associated with alternative methods necessary for removing entrapped catheters. In the event of catheter retainment, using the Apollo™ Onyx™ Delivery Microcatheter versus any a standard catheter represents leaving behind a 1.5 - 3.0 cm long detachable tip in the Onyx™ Onyx™ Delivery Microcatheter cast versus an average 165 cm long catheter in the vasculature. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02378883
Study type	Interventional
Source	Medtronic Neurovascular Clinical Affairs
Contact
Status	Completed
Phase	N/A
Start date	May 18, 2015
Completion date	February 20, 2018

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