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SMART: A prospective, multi-center registry assessing the embolization of neurovascular lesions using the Penumbra SMART COIL? System

Study category: Bones, Muscles, and Joints

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Description

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.

Details
Age

Adult

Eligibility

Intracranial aneurysm; other neurovascular abnormalities such as arteriovenous malformations and ateriovenous fistulae

Phase

Not Applicable - Describes studies without FDA-defined phases, including studies of devices or behavioral interventions.

Type of Study

Observational

Location

University of Colorado Hospital

Principal Investigator
David Case,  MD

David Case, MD

Study ID

Protocol Number: 17-2122

ClinicalTrials.gov: NCT02729740

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