Visceral Artery Aneurysm Embolization by the Penumbra Ruby™ Coil System

Status Withdrawn

Clinical Trial Summary

The primary objective of this study is to gather post market data on the Penumbra Ruby Coil System in the treatment of visceral artery aneurysms and arteriovenous malformations. This study is a prospective, multi-center study of patients with visceral artery aneurysms and visceral arteriovenous malformations who are treated by the Penumbra Ruby Coil System. Data for each patient are collected up to 12 months post-procedure for the study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02079818
Study type	Interventional
Source	Penumbra Inc.
Contact
Status	Withdrawn
Phase	Phase 4
Start date	June 2017
Completion date	September 2018

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