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Sleep Quality and Sleep-disordered Breathing in Bypass Surgery Patients

Patients undergoing non-emergency coronary artery bypass surgery (CABG) are included. All patients will be examined for transthoracic echo, blood samples will be collected, and an overnight sleep polygraph will be performed in a qualified sleep laboratory twice: once before CABG and again after surgery

Condition(s)Sleep Disorder, Coronary Artery Disease
StatusRecruiting
Study typeObservational
SummaryPatients undergoing non-emergency coronary artery bypass surgery (CABG) are included. All patients will be examined for transthoracic echo, blood samples will be collected, and an overnight sleep polygraph will be performed in a qualified sleep laboratory twice: once before CABG and again after surgery
Who can participateInclusion Criteria: Elective coronary artery bypass surgery Exclusion Criteria: * Emergency cabg * Night time cpap- treatment * other heart operations (for example valve surgery)
Ages18 Years to 90 Years
SexAll
Lead sponsorTurku University Hospital
LocationsTurku, Finland
Start date2023-02-01
NCT IDNCT06453538
Official listinghttps://clinicaltrials.gov/study/NCT06453538

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