The SMARTER Cardiomyopathy Study
NCT05750147 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2024-03-06
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.
Conditions
- Cardiomyopathies
- Hypertrophic Cardiomyopathy
- Dilated Cardiomyopathy
Interventions
- OTHER
-
Blood Sample Collection
Blood for DNA and biomarker analysis
Sponsors & Collaborators
-
Imperial College London
lead OTHER
Principal Investigators
-
James Ware · Imperial College London
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-03-01
- Primary Completion
- 2027-08-01
- Completion
- 2027-08-01
Countries
- United Kingdom
Study Locations
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