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FIrst-Pass Reperfusion With the NeVa Stent-Retriever Trial — FIRST  

Acute Ischemic Stroke Clinical Trial

Official title:
A Prospective, Randomized, Open-Label, Multi-Center, Assessor-Blinded Study Designed to Compare the Safety, Performance and Efficacy of the NeVatm Stent Retriever Versus the Solitairetm Stent Retriever

Clinical Trial Summary

This study is designed to compare the safety, performance and efficacy of blood clot (thrombus) removal in subjects presenting with acute ischemic stroke with the NeVa versus the Solitaire stent retrievers.

Clinical Trial Description

A pivotal, randomized, open label, assessor-blinded, 90-day study designed to compare the safety, performance and efficacy of thrombus removal in subjects aged ≥ 18 years presenting with acute ischemic stroke with the NeVa versus the Solitaire stent retrievers. A total of 414 eligible subjects will be randomized in a 1:1 ratio to one of two treatment groups: - Active Treatment Group - Control Device ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04072367
Study type Interventional
Source Vesalio
Contact
Status Withdrawn
Phase N/A
Start date December 2020
Completion date December 2020
View Details
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