This is a prospective, multi-center registry of patients treated in accordance with the cleared indications for the Smart, Penumbra Coil 400, and the Penumbra Occlusion Device. Data for each patient are collected in accordance with the standard of care at each participating hospital through one-year follow-up.More
Intracranial aneurysm; other neurovascular abnormalities such as arteriovenous malformations and ateriovenous fistulae
Not Applicable - Describes studies without FDA-defined phases, including studies of devices or behavioral interventions.
University of Colorado Hospital
David Case, MD
Protocol Number: 17-2122
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