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EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysms With the Pipeline™ Flex Embolization Device With Shield TEchnology™ (ELEVATE) — ELEVATE  

Intracranial Aneurysm Clinical Trial

Official title:
EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysms With the Pipeline™ Flex Embolization Device With Shield TEchnology™ (ELEVATE)

Clinical Trial Summary

The purpose of the study is to assess the safety and effectiveness of the Pipeline™ Flex Embolization Device with Shield Technology™ in the treatment with acutely ruptured intracranial aneurysms.

Clinical Trial Description

The ELEVATE study is a prospective, multi-center, single-arm trial of the Pipeline™ Shield Device for the treatment of adults with acutely ruptured intracranial aneurysms. The primary objective of the ELEVATE study is to assess the safety and effectiveness of treatment with the Pipeline™ Shield Device of acutely ruptured intracranial aneurysms that are not amenable for clipping and coiling. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04391803
Study type Interventional
Source Medtronic Neurovascular Clinical Affairs
Contact Medtronic Neurovascular Clinical Affairs
Phone 949-837-3700
Email rs.elevate@medtronic.com
Status Recruiting
Phase N/A
Start date May 6, 2022
Completion date January 2027
View Details
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