Last updated on November 2018

Safety and Efficacy of the LVIS and LVIS JR Devices in the Endovascular Treatment of Intracranial Aneurysms

Brief description of study

A French, multicenter, prospective, observational, "real life" assessment of the safety and efficacy of LVIS and LVIS JR devices in the treatment of intracranial aneurysms

Detailed Study Description

This is a multicenter observational study. Treatment and follow-up visits will be done as per standard of care.

The purpose of this study is to collect data on safety of the devices used since the French reimbursement.

130 patients will be enrolled over an 18-month recruitment period. All patients will be followed for at least 12 months.

Clinical Study Identifier: NCT03553771

Contact Investigators or Research Sites near you

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Arturo Consoli, MD

H pital Foch
Suresnes, France
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Recruitment Status: Open

Brief Description Eligibility Contact Research Team

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