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Registry on NeVa VS for CerebraL VAsospasm ManagemenT in Post SAH PatiEnts
Sponsor: Vesalio
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
2026-05-27
Healthy Volunteers
No
Interventions
NEVA VS
cerebral artery dilation device
Locations (16)
Providence St. Joseph Medical Center
Burbank, California, United States
John Muir Health
Walnut Creek, California, United States
Yale
New Haven, Connecticut, United States
Baptist Health South Florida
Miami, Florida, United States
Wellstar Health System
Marietta, Georgia, United States
Endeavor Health
Evanston, Illinois, United States
Univ Iowa
Iowa City, Iowa, United States
Univ Kentucky
Lexington, Kentucky, United States
MaineHealth
Portland, Maine, United States
Mayo Clinic- Rochester
Rochester, Minnesota, United States
Allegheny Health Network
Pittsburgh, Pennsylvania, United States
Geisinger
Wilkes-Barre, Pennsylvania, United States
Valley Baptist Medical Center- Harlingen
Harlingen, Texas, United States
University of Texas Health Science Center at Houston
Houston, Texas, United States
Uni. of Utah
Salt Lake City, Utah, United States
West Virginia University
Morgantown, West Virginia, United States