Postoperative Atrial Fibrillation
Conditions
Brief summary
Assessment of Postoperative atrial fibrillation incidence, by Holter monitoring
Detailed description
The secondary trial endpoints are assessments of activation of HSPs by biochemical analysis and microscopic imaging; in blood, atrial tissue and epicardial adipose tissue
Interventions
Sponsors
Stichting Amsterdam UMC
Eligibility
Sex/Gender
All
Age
18 Years to 64 Years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of Postoperative atrial fibrillation incidence, by Holter monitoring | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary trial endpoints are assessments of activation of HSPs by biochemical analysis and microscopic imaging; in blood, atrial tissue and epicardial adipose tissue | — |
Countries
Netherlands
Outcome results
None listed