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NOT YET RECRUITING
NCT06893588
Registry on NeVa VS for CerebraL VAsospasm ManagemenT in Post SAH PatiEnts
Sponsor: Vesalio
View on ClinicalTrials.gov
Summary
A multi-center, observational registry study intended to assess the HDE-approved NeVa VS cerebral artery dilation device in patients with symptomatic cerebral vasospasm caused by aneurysmal subarachnoid hemorrhage (aSAH)
Official title: Prospective, Open-Label, Multi-Center ProceDural Data CollectIon Case Registry on NeVa VS for CerebraL VAsospasm ManagemenT in Post SAH PatiEnts (The DILATE Registry)
Key Details
Gender
All
Age Range
22 Years - Any
Study Type
OBSERVATIONAL
Enrollment
200
Start Date
2025-04-14
Completion Date
2027-03-15
Last Updated
2025-03-25
Healthy Volunteers
No
Interventions
DEVICE
NEVA VS
cerebral artery dilation device