Goal of the study is to evaluate the efficacy and safety of acute permanent stenting of symptomatic intracranial stenosis following unsuccessful recanalization by thrombectomy in acute ischemic stroke with large vessel occlusion using the self-expandable CREDO® heal Stent.
Study Type
OBSERVATIONAL
Enrollment
153
Rescue stenting with CREDO heal Stent together with NeuroSpeed PTA Balloon Catheter
Institut für Radiologie und Neuroradiologie, Klinikum Aschaffenburg-Alzenau
Aschaffenburg, Germany
Primary Technical Efficacy Endpoint- proportion of patients with eTICI 2b-3 at the end of the treatment procedure.
• Technical success defined as successful recanalization of the occluded vessel (expanded treatment in cerebral ischemia score (eTICI) of 2b-3) at the end of the procedure.
Time frame: Assessed at the end of the treatment procedure.
Primary Clinical Efficacy Endpoint- proportion of patients with mRS 0-2 at 90 (± 20) days after procedure.
• Good clinical outcome 90 (± 20) days after stroke defined as a score of 0-2 on the modified Ranking Scale (mRS 0-2).
Time frame: 90 (± 20) days.
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