About this trial
The goal of this observational study is to evaluate the role of blood pressure (BPV) variability in patients suffering from acute ischemic stroke. The main questions it aims to answer are:
1. To determine the association of BPV with functional/cognitive outcome after ischemic stroke. 2. To determine a pathophysiologic mechanism of BPV's deleterious effect on functional outcome. 3. To evaluate potential treatment targets to pharmacologically reduce BPV after ischemic stroke.
Eligibility criteria
Qualifiers
CT or MRI showing ischemic stroke in the anterior circulation (frontal, parietal or superior temporal lobes), or
Occlusion of the internal carotid, middle cerebral or anterior cerebral arteries on computed tomography angiography (CTA) or magnetic resonance angiography (MRA)
Disqualifiers
Pre-morbid mRS ≥3
Predicted hospital system admission <72 hours
Pacemaker or other MRI contraindications per American College of Radiology guidelines
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Yale University
Lead sponsor
University of Chicago
Collaborator
Massachusetts General Hospital
Collaborator
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborator