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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.

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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.

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Contacts and locations

Locations

  • Glenfield Hospital

    Leicester, LE3 9QP, United Kingdom

  • Leeds Teaching Hospitals NHS Trust

    Leeds, LS1 3EX, United Kingdom

  • Liverpool Heart and Chest Hospital NHS Foundation Trust

    Liverpool, L14 3PE, United Kingdom

  • Oxford University Hospitals NHS Foundation Trust

    Oxford, United Kingdom

  • Royal Brompton & Harefield NHS Foundation Trust

    London, SW3 6NP, United Kingdom

  • Southampton General Hospital

    Southampton, SO16 6YD, United Kingdom

Conditions

Explore the condition pages connected to this study.