A prospective, multicenter, observational assessment of the safety and effectiveness of the LVIS® device in the treatment of wide necked intracranial aneurysms.
Study Type
OBSERVATIONAL
Enrollment
90
Low-profile Visualized Intraluminal Support device
Anatomical stability of aneurysm treatment compared to the initial occlusion rate of the aneurysm
Time frame: 6 months
Anatomical stability of aneurysm treatment compared to the initial occlusion rate of the aneurysm
Time frame: 18 months
Retreatment rate
Time frame: 6 months
Retreatment rate
Time frame: 18 months
Morbidity rate
Time frame: 6 months
Morbidity rate
Time frame: 18 months
Mortality rate
Time frame: 6 months
Mortality rate
Time frame: 18 months
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