UnknownNot Applicable

Sleep-disordered Breathing and Perioperative Atrial Fibrillation in Cardiac Surgery

Germany1,200 participantsStarted 2016-07

Plain-language summary

In patients undergoing elective coronary artery bypass grafting (CABG) surgery, coronary artery disease, sleep-disordered breathing (SDB), atrial fibrillation (AF) perioperative atrial fibrillation and complications will be assessed. The primary objective is to determine, whether SDB patients have a higher rate of Major Adverse Cardiac and Cerebrovascular Events (MACCE) within 30 days after surgery compared to those without SDB.

Who can participate

Age range18 Years – 85 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients undergoing elective CABG surgery at the Department of Cardiac and Thoracic Surgery, University Hospital Regensburg. * Written informed consent Exclusion Criteria: * Preoperative use of inotropes or intra aortic balloon pump * Severe obstructive pulmonary disease * Patients on oxygen therapy, nocturnal positive airway pressure support or mechanical ventilation

What they're measuring

Major Adverse Cardiac and Cerebrovascular Events (MACCE)

Timeframe: 30 days

Trial details

NCT IDNCT02877745

SponsorMichael Arzt

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-05

Contact for this trial

Michael Arzt, MD

+49 941 944 7281 michael.arzt@ukr.de

View on ClinicalTrials.gov More Elective Coronary Artery Bypass Grafting (CABG) Surgery trials