The National SMuRFless CAD Registry
The national SMuRFless CAD Registry is a multi-centre, prospective, observational cohort study of SMuRFless patients attending a SMuRFless CAD Clinic. Through the establishment of the SMuRFless CAD Registry, we gather information on less common risk factors for CAD and assess the effectiveness of targeting these factors in preventing heart attacks. By participating in the registry, you contribute to identifying new risk factors and potential treatments to reduce the risk of future heart attacks. This information also helps us develop evidence-based care pathways for individuals with CAD who do not have standard risk factors. Our clinic, funded by the Australian Government, is part of the NHMRC CRE for CAD initiative, led by a network of internationally recognised CAD experts. Together, we strive to improve the diagnosis, treatment, and quality of care for people with CAD.
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Your contributions as a SMuRFless CAD Registry participant:
Uncover new or less commonly known risk factors for CAD that can contribute to a better understanding of the disease.
Contribute to reducing the future risk of heart attacks by studying the effectiveness of targeted interventions.
Inform the development of evidence-based care pathways specifically tailored for individuals with CAD without SMuRFs