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Clinical Trial Summary

A post-market registry evaluating the EmboTrap® Revascularization Device and CERENOVUS Large Bore Catheter/ EMBOVAC Aspiration Catheter in acute ischemic stroke patients with confirmed intracranial large vessel occlusion.


Clinical Trial Description

The objective of this study are to separately assess the effectiveness of the CERENOVUS neurothrombectomy devices (EmboTrap® Revascularization Device, and Large Bore Catheter/EMBOVAC Aspiration Catheter) in a real-world setting, as well as to explore correlations between patient comorbidities, clot characteristics, revascularization rates, and clinical outcomes.. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03685578
Study type Observational
Source Cerenovus, Part of DePuy Synthes Products, Inc.
Contact Erin O'Carroll- Godinez
Phone +1 949-433-9824
Email EOCarro3@its.jnj.com
Status Recruiting
Phase
Start date September 28, 2018
Completion date October 1, 2024

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