A multi-site, multi-modality prospective observational clinical outcomes study focussed on the development of phenotype-dirven risk prediction modelling in patients with known or suspected cardiovascular disease.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* All patients referred for hospital-based cardiac imaging services
Exclusion Criteria:
* Failure or provide informed consent
Primary outcome measure(s)
Major adverse cardiovascular outcomes (MACE) — 2024 Composite of all-cause death, heart failure admission, myocardial infarction, heart transplantation or LVAD, Stroke or TIA
Malignant arrhythmic events — 2024 Composite of sudden cardiac death or appropriate ICD shock
Heart failure events — 2024 Composite of heart failure admission, death or need for transplantation / LVAD
Atrial arrhythmic events — 2024 Occurrence of atrial fibrillation / atrial flutter (documented by 12-lead ECG or Holter monitor)
All-cause mortality — 2024 Death based on Vital Statistics Alberta and In-hospital coded death
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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