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Elektrode studie.

Recruiting
Conditions
Epicardial, Mapping, Atrial Fibrillation, Cardiac Surgery
Registration Number
NL-OMON26202
Lead Sponsor
Erasmus MC Rotterdam The Netherlands
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

All patients > 18 years scheduled for standard coronary bypass grafting.

Exclusion Criteria

1. Paced atrial rhythms;

2. Usage of anti-arrhythmic drugs;

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The main endpoint of the study is reached when atrial fibrillation develops. There is a follow-up period of 5 years after<br>cardiac surgery. Each year, the participant will be called by the investigator in order to check whether atrial fibrillation has<br>occurred.
Secondary Outcome Measures
NameTimeMethod
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