A prospective, open label 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 registry designed to assess the safety, performance and efficacy of the NeVa stent retriever in the treatment of large vessel occlusion strokes. Up to 600 subjects will be enrolled at up 30 sites.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
600
mechanical neurothrombectomy
Hospital Espanol de Mendoza
Mendoza, Argentina
RECRUITINGNiguarda Hospital
Milan, Italy
RECRUITINGCleveland Clinic Abu Dhabi
Abu Dhabi, United Arab Emirates
RECRUITINGFirst Pass Success Rate
The primary study endpoint is the first pass success rate with the NeVa device defined as eTICI score ≥ 2B \& eTICI ≥2C
Time frame: post-procedure day 0
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.