Ischemic Stroke Clinical Trial
Official title:
A Prospective, Multicenter, Observational, Single-arm European Registry on the ACE Reperfusion Catheters and the Penumbra System in the Treatment of Acute Ischemic Stroke
Prospective, single-arm, multicenter, observational registry of the ACE Reperfusion Catheters and the Penumbra System in Europe. Consecutive patients presenting within 6 hours from symptom onset with an acute ischemic stroke (within the internal carotid artery and internal carotid terminus, middle cerebral - M1/M2 segments) due to anterior circulation large vessel occlusion (LVO) will be treated using the ADAPT technique with thrombo-aspiration as first intention and site routine practice.
Prospective, single-arm, multicenter, observational registry of the ACE Reperfusion Catheters
and the Penumbra System in Europe. Consecutive patients presenting within 6 hours from
symptom onset with an acute ischemic stroke (within the internal carotid artery and internal
carotid terminus, middle cerebral - M1/M2 segments) due to anterior circulation large vessel
occlusion (LVO) will be treated using the ADAPT technique with thrombo-aspiration as first
intention and site routine practice.
The follow-up visit will occur 24 hours, 7-10 days or discharge, 30 days and 90 days
post-procedure and will review patient's functional outcome, quality of life, and adverse
events.
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