SMART: A prospective, multi-center registry assessing the embolization of neurovascular lesions using the Penumbra SMART COIL? System
This Study is
No Longer Enrolling
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.
MoreAdult
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.
Observational
University of Colorado Hospital
Protocol Number: 17-2122
More information available at ClinicalTrials.gov: NCT02729740
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