Last updated on June 2017

AneuRysm Treatment using IntraSaccular Flow DiverSion with the ArtissE™ Device


Brief description of study

AneuRysm Treatment using IntraSaccular Flow DiverSion with the ArtissE™ Device

Detailed Study Description

This study is a prospective, multi-center, single-arm study. Subjects requiring treatment for a single de novo unruptured or ruptured (having occurred within the 60 days prior to treatment), wide-neck bifurcating or branching saccular aneurysm will be enrolled.

Clinical Study Identifier: TX150557

Contact Investigators or Research Sites near you

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Sara Renfrow

Baptist Health Lexington Clinical Research Center
Lexington, KY USA
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Recruitment Status: Open


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