Post-Operative Myocardial Incident & Atrial Fibrillation

Recruiting Observational Study
Valve Heart Disease Coronary Artery Disease
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
1,500 (estimated)
Sponsor
University Hospital, Lille · Other
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About This Trial

To explore predictors of major cardio-vascular events after cardiac surgery and trans-catheter valve implantation with a specific interest in studying mechanisms linking pre-operative leukocyte, fat and myocardial phenotypes with post-intervention outcomes.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * patients scheduled for cardiac surgery (coronary artery bypass graft surgery and/or valvular surgery) or transcatheter valve implantation Exclusion Criteria: * pregnant woman * urgent surgery or intervention * not able to consent to the protocol
Contacts

David Montaigne, Prof.

320445230

david.montaigne@chru-lille.fr

CONTACT