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Clinical Trial Summary

The purpose of this study is to determine whether treatment of obstructive sleep apnea (OSA) with positive airway pressure starting shortly after acute ischemic stroke or high risk TIA (1) reduces recurrent stroke, acute coronary syndrome, and all-cause mortality 6 months after the event, and (2) improves stroke outcomes at 3 months in patients who experienced an ischemic stroke.


Clinical Trial Description

Sleep SMART has a prospective, randomized, open-label, blinded-endpoint (PROBE) design. It is a multi-site, parallel-group superiority trial that compares 6 months of OSA treatment to usual care. The study includes two trials: a prevention study with an embedded recovery trial. 3062 subjects will be randomized over 5 years at 110 sites within the NINDS-funded StrokeNet clinical trials network. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03812653
Study type Interventional
Source University of Michigan
Contact Kayla Novitski, MPH, CCRP
Email kcgossel@med.umich.edu
Status Recruiting
Phase N/A
Start date May 9, 2019
Completion date November 2026

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