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Sleep-disordered Breathing and Perioperative Atrial Fibrillation in Cardiac Surgery (CONSIDER-AF)

M

Michael Arzt

Status

Unknown

Conditions

Coronary Artery Disease
Atrial Fibrillation
Elective Coronary Artery Bypass Grafting (CABG) Surgery
Sleep-disordered Breathing (SDB)

Treatments

Other: Stratification, no intervention

Study type

Observational

Funder types

Other

Identifiers

NCT02877745
3643420

Details and patient eligibility

About

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.

Enrollment

1,200 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

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

Trial design

1,200 participants in 2 patient groups

no SDB
Description:
apnea-hyponea index \<15/hour
Treatment:
Other: Stratification, no intervention
SDB
Description:
apnea-hyponea index \>=15/hour
Treatment:
Other: Stratification, no intervention

Trial contacts and locations

1

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Central trial contact

Michael Arzt, MD; Stefan Wagner, MD

Data sourced from clinicaltrials.gov

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