50
Participants
Start Date
April 22, 2016
Primary Completion Date
June 16, 2017
Study Completion Date
June 18, 2018
ApneaLink Plus, BIA Device
The study is only observational. No interventions will be performed. ApneaLink Plus will be used to diagnose Obstructive Sleep Apnea in potential candidates and grade its severity on Postoperative night 2 in participants. A BIA Device will be used to detect segmental fluid shifts. A 3-D accelerometer will be used to detect head and neck position.
Toronto Western Hospital- UHN, Toronto
Society of Anesthesia and Sleep Medicine
UNKNOWN
University Health Network, Toronto
OTHER