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)
Study Type
OBSERVATIONAL
Enrollment
200
cerebral artery dilation device
Providence St. Joseph Medical Center
Burbank, California, United States
RECRUITINGJohn Muir Health
Walnut Creek, California, United States
Improvement in target vessel diameter following NeVa VS use
Time frame: Up to 1 hour post procedure
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Yale
New Haven, Connecticut, United States
RECRUITINGBaptist Health South Florida
Miami, Florida, United States
RECRUITINGWellstar Health System
Marietta, Georgia, United States
RECRUITINGEndeavor Health
Evanston, Illinois, United States
RECRUITINGUniv Iowa
Iowa City, Iowa, United States
RECRUITINGUniv Kentucky
Lexington, Kentucky, United States
RECRUITINGMaineHealth
Portland, Maine, United States
RECRUITINGMayo Clinic- Rochester
Rochester, Minnesota, United States
RECRUITING...and 6 more locations