Aneurysms Clinical Trial
Official title:
Cordis Neurovascular Feasibility Study of the Enterprise Self-Expanding Stent System to Facilitate Endovascular Coil Embolization of Wide- Neck Saccular Intracranial Artery Aneurysms
To evaluate the safety and feasibility of the Cordis Neurovascular Self-Expanding Stent
System to facilitate endovascular coil embolization of wide neck saccular intracranial
aneurysms.
Cordis Self Expanding Stent for use with embolic coils for the treatment of wide-neck,
intracranial, saccular aneurysms arising from a parent vessel
This is a multi-center, prospective, non-randomized feasibility study including 30 subjects. Subjects will receive a safety follow-up evaluation at 30 days (+ two weeks) and an efficacy follow-up evaluation at 6 months (+ four weeks). ;
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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