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Contour Neurovascular System - European Pre-Market Unruptured Aneurysm — CERUS  

Intracranial Aneurysm Clinical Trial

Official title:
Contour Neurovascular System - European Pre-Market Unruptured Aneurysm Study (CERUS)

Clinical Trial Summary

Cerus Endovascular is sponsoring a prospective, multi-center trial to document the safety and performance of the Contour Neurovascular System™ ("Contour"). The purpose of the study is to document safety and performance of the Contour in treatment for patients with intracranial aneurysms (IA). The data from the study will be reported as a Pre-Market study to the Notified Body to support CE Mark approval.

Clinical Trial Description

Contour Neurovascular System™ European Pre-Market Unruptured Aneurysm Study (CERUS) initiated enrollment in October 2018 to assess the safety and effectiveness of the Contour Neurovascular System ("Contour") in treatment of intracranial aneurysms (IA) with the intended indication for endovascular embolization of saccular IA. This prospective, single-arm, multicenter study was conducted to document the safety and performance of the Contour in treatment for patients with an IA. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03680742
Study type Interventional
Source Cerus Endovascular, Ltd
Contact
Status Completed
Phase N/A
Start date September 18, 2018
Completion date February 2, 2021
View Details
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