Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to gather safety and effectiveness data on Stryker Neurovascular's Next Generation Target Detachable Coil (hereafter referred to as the Citadel Embolization Device), when used with Target Detachable Coils, in the treatment of wide-neck intracranial aneurysms.


Clinical Trial Description

In this study, use of the Citadel Embolization Device will be limited to a population of patients with unruptured or ruptured wide-neck aneurysms who meet all study eligibility criteria. The Citadel Embolization Device is intended to endovascularly obstruct or occlude blood flow in intracranial aneurysms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04057352
Study type Interventional
Source Stryker Neurovascular
Contact John Strohmeyer
Phone 267-337-5012
Email john.strohmeyer@stryker.com
Status Recruiting
Phase N/A
Start date July 17, 2019
Completion date March 30, 2027