Subarachnoid Hemorrhage Clinical Trial
Official title:
Lumenate Observational Vasospasm Interventional Trial (LOVIT)
The LOVIT study is a European prospective, multi-center, open-label, single-arm feasibility trial designed to determine the safety and angiographic effectiveness through 30 days post treatment with Lumenate Intraluminal Device in the treatment of symptomatic vasospasm.
The Neurvana Lumenate Intraluminal Device is delivered via a percutaneous endovascular
approach to the target segment for mechanical assistance and the treatment of vasospasm.
The LOVIT study is a European prospective, multi-center, open-label, single-arm feasibility
trial designed to determine the safety and angiographic effectiveness through 30 days post
treatment with Lumenate Intraluminal Device in the treatment of symptomatic vasospasm. The
primary objective of the study is to support the CE-mark vasospasm label claim for the
Lumenate Device. The study will be enrolled at up to 8 European sites with study subjects
being followed for 90 days post-treatment.
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