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The SMARTER Cardiomyopathy Study
Sponsor: Imperial College London
Summary
Cardiomyopathies are diseases of the heart muscle. Known genetic factors may account for some cardiomyopathy cases but there is still much to understand about the genetic and environmental causes and how the disease progresses. Finding new ways to diagnose and treat cardiomyopathies could improve the health and well-being of patients with these conditions. This study will collect data from individuals with cardiomyopathy or related heart muscle disease, or with a possible genetic predisposition to cardiomyopathy, and follow them over time to observe the progress of their heart and health. This study will collect DNA, blood samples, and detailed clinical \& lifestyle information at the start of the study, and data collected during routine healthcare visits over time. * learn what causes cardiomyopathy, and therefore how to treat it * understand why cardiomyopathy progresses differently in different people, to improve the ability to recognise who will benefit from different treatments at different times The investigators will collaborate with other centres internationally to collect a large of group of participants with similar cardiomyopathies, providing power to identify new pathways that cause disease and ways of predicting which participants are at risk of having more severe disease.
Official title: Genetics, Imaging and Artificial Intelligence for Precision Care in Cardiomyopathy
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
1000
Start Date
2023-03-01
Completion Date
2027-08-01
Last Updated
2024-03-06
Healthy Volunteers
No
Interventions
Blood Sample Collection
Blood for DNA and biomarker analysis
Locations (2)
Guys & St Thomas' NHS Foundation Trust
London, United Kingdom
Kings College Hospital
London, United Kingdom