The goal of this observational study is to establish a prospective multicenter registry of patients undergoing intracranial stenting for ischemic strokes caused by medically refractory ICAD. The study aims to evaluate current practice patterns, periprocedural outcomes, and delayed outcomes. Researchers will collect demographic and procedural data from patients who undergo intracranial stenting after having an ischemic stroke caused by medically refractory ICAD.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Recurrent ischemic stroke within treated territory, ICH, or death
Timeframe: 72 hours post procedure
Stroke, ICH, or neurological death in treated territory
Timeframe: 6 months to 1 year post procedure