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Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data Collection

Cerebral Aneurysm Clinical Trial

Official title:
Prospective, Observational, Multi-Center, Single-Arm, Consecutive Enrollment, Post-Marketing, International Registry of the Surpass™ Flow Diverter in Intracranial Arteries

Clinical Trial Summary

The purpose of this observational post-marketing registry will be to collect and analyze safety, effectiveness, and quality of life outcomes, during and after treatment with the Surpass Flow Diverter. Health Economics assessments (cost data) will also be collected and analyzed.

Clinical Trial Description

This will be a prospective, observational, multi-center, single-arm, post-marketing, international registry with consecutive enrollment of a minimum of 150 patients treated with the Surpass Flow Diverter in accordance with the standard of care at up to 30 registry sites. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02281721
Study type Observational [Patient Registry]
Source Stryker Neurovascular
Contact
Status Terminated
Phase
Start date March 18, 2015
Completion date December 2019
View Details
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