Exploring heart event predictors after cardiac surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to identify predictors of major cardiovascular events following cardiac surgery and trans-catheter valve implantation. It focuses on understanding how pre-operative factors such as leukocyte counts, fat distribution, and myocardial characteristics relate to outcomes after these interventions. By analyzing these connections, the study seeks to improve prognostic assessments for patients undergoing cardiac procedures.

Why it matters

Who can join: the full rules

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

Where it's running

• Hôpital Cardiologie, CHU
  Lille, France Recruiting

Study contacts

• Principal investigator: David Montaigne, Prof. — University Hospital, Lille
• Study coordinator: David Montaigne, Prof.
• Email: david.montaigne@chru-lille.fr
• Phone: 320445230

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.