Versi Retriever Approving Trial in Japan

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

This is Versi Retriever mechanical thrombectomy device approving study in Japan. Multi center, single arm, prospective registry trial. Physicians control trial, conducted my N Sakai, Kobe City Medical Center General Hospital. 60 cases will be enrolled and 90 days follow up need. Primary endpoint is favorable clinical outcome, mRS 0-2. Secondary endpoint are mortality in 90days, immediate successful recanalization, TICI 2b-3, symptomatic intracranial hemorrhage, and any adverse event related to device and or procedure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04129203
Study type	Interventional
Source	Kobe City General Hospital
Contact	Nobuyuki Sakai, MD DMSc
Phone	81783024321
Email	n.sakai@siren.ocn.ne.jp
Status	Recruiting
Phase	N/A
Start date	February 1, 2019
Completion date	December 31, 2021

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