A prospective, open label, single-arm 90-day study designed to assess the safety, performance and efficacy of thrombus removal in subjects presenting with acute ischemic stroke with the NeVa stent retrievers.
This is a prospective, open label, multi-center, single-arm trial designed to assess the safety, performance and efficacy of the NeVa stent retriever in the treatment of large vessel occlusion strokes. Up to 120 eligible subjects at up 20 sites will participate in the study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
120
mechanical neurothrombectomy
Vascular Neurology of Southern California
Thousand Oaks, California, United States
Baptist Health Research Institute
Jacksonville, Florida, United States
WellStar System Inc
Marietta, Georgia, United States
Community Hospital
Munster, Indiana, United States
Recanalization rate of the occluded target vessel
Recanalization rate of the occluded target vessel (defined by an eTICI score ≥ 2b) following three or less passes using the NeVa device(s).
Time frame: During the procedure/surgery
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University of Maryland Medical Center Dept of Diagnostic Radiology & Nuclear Med.
Baltimore, Maryland, United States
Fort Sanders Regional
Knoxville, Tennessee, United States
Texas Tech University Health
El Paso, Texas, United States