NCT03376165Recruiting
Post-Operative Myocardial Incident & Atrial Fibrillation
Longitudinal Study of Patients Undergoing Cardiac Surgery or Implantation of a Percutaneous Valve Prosthesis
Source: ClinicalTrials.gov · Last updated 14 May 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 1500 (estimated)
- First submitted
- 11 Dec 2017
- Start date
- 30 Jan 2018
- Primary completion date
- 31 Jan 2028
- Lead sponsor
- University Hospital, Lille
- NCT number
- NCT03376165
What you commit to
- Study type: Observational
- Planned participants: 1500
- From 30 Jan 2018 to the primary completion date, 31 Jan 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- urgent surgery or intervention
Other
- pregnant woman
- not able to consent to the protocol
Who the study is looking for
- patients scheduled for cardiac surgery (coronary artery bypass graft surgery and/or valvular surgery) or transcatheter valve implantation
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hôpital Cardiologie, CHU Coordinator of this site? Confirm its status | Lille | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.