Epicardial Mapping Studies in Patients undergoing Cardiac Surgery Roepnaam Quasar

Completed

• Conditions: atrial fibrillation; 10007521; 10007593

• Registration Number: NL-OMON39666
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2020-04-20
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 650

Inclusion Criteria

All patients > 18 years scheduled for standard cardiac surgery.

Exclusion Criteria

paced atrial rhythms
usage of anti-arrhythmic drugs
hemodynamic instability
presence of assist devices
usage of inotropic agents
emergency cardiac surgery
redo-cardiac surgery

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main endpoint of the study is reached when atrial fibrillation develops.<br /><br>There is a follow-up period of 5 years after cardiac surgery. Each year, the<br /><br>participant will be called by the investigator in order to check whether atrial<br /><br>fibrillation has occurred.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>NA</p><br>