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Vesalio NeVa VS for Symptomatic Cerebral Vasospasm Following aSAH (The VITAL Study)

Cerebral Vasospasm Clinical Trial

Official title:
The Vesalio Neva VS for the Treatment of Symptomatic Cerebral Vasospasm Following Aneurysmal Subarachnoid Hemorrhage (aSAH) (The VITAL Study)

Clinical Trial Summary

The objective of the study is to assess the safety and probable benefit of the Neva VS device in patients presenting with symptomatic cerebral vasospasm despite maximal medical management following aSAH.

Clinical Trial Description

This is a prospective, open label, single-arm study. Up to 30 eligible subjects at up to 15 sites will participate in the study. Subjects will be followed up for 30 days post-intervention. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03611790
Study type Interventional
Source Vesalio
Contact
Status Completed
Phase N/A
Start date December 19, 2018
Completion date May 31, 2021
View Details
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