Heart disease mystery: 2000 patients join quest for genetic clues
NCT ID NCT03843255
First seen Apr 04, 2026 · Last updated Apr 30, 2026 · Updated 6 times
Summary
This study follows 2000 people with dilated cardiomyopathy, a condition where the heart becomes enlarged and weak. Researchers collect blood for genetic testing and perform heart MRI scans to look for scarring. The goal is to find genetic changes and heart damage patterns that could lead to better diagnosis and personalized treatments in the future.
Disclaimer
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This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Locations
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Glenfield Hospital
Leicester, LE3 9QP, United Kingdom
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Leeds Teaching Hospitals NHS Trust
Leeds, LS1 3EX, United Kingdom
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Liverpool Heart and Chest Hospital NHS Foundation Trust
Liverpool, L14 3PE, United Kingdom
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Oxford University Hospitals NHS Foundation Trust
Oxford, United Kingdom
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Royal Brompton & Harefield NHS Foundation Trust
London, SW3 6NP, United Kingdom
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Southampton General Hospital
Southampton, SO16 6YD, United Kingdom
Conditions
Explore the condition pages connected to this study.