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Keep this study
Lead
Medtronic Neurovascular Clinical Affairs
This is a prospective, multi-center, non-randomized observational registry evaluating use of BOSS balloon guide catheters in patients diagnosed with an acute ischemic stroke due to large intracranial vessel occlusion.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Acute ischemic stroke vessel occlusion (ICA, M1 or M2) of the anterior circulation with associated symptoms
Adult patient willing to provide Informed Consent
Pre-treatment National Institutes of Health Stroke Scale (NIHSS) ≥ 6
You may not be if
Posterior circulation stroke
Tandem occlusions
Cervical carotid stenosis
Participating in another clinical trial
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