Heart disease detective: 1,000-Person study hunts for hidden genetic triggers of sudden cardiac death

NCT ID NCT03049254

First seen Jun 27, 2026 ยท Last updated Jun 27, 2026

Summary

This study is looking for new genes and blood markers linked to arrhythmogenic cardiomyopathy (AVC), a genetic heart condition that can lead to heart failure and sudden cardiac arrest. Researchers will enroll 1,000 people, including patients with AVC or unexplained cardiac arrest, and their blood relatives. By collecting medical data, images, and samples, they hope to better understand how the disease starts and progresses, which could improve diagnosis and screening for at-risk families.

What this could mean

Our plain-language read of the trial. This is informational only โ€” not medical advice or a prediction.

What this could lead to
If successful, this could lead to better genetic tests and early detection methods for arrhythmogenic cardiomyopathy, potentially preventing sudden cardiac death in at-risk families.
What could go wrong
This is an observational study, not a treatment trial. It may not directly benefit participants, and findings may take years to translate into clinical practice.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Mayo Clinic

    RECRUITING

    Rochester, Minnesota, 55905, United States

  • Royal Papworth Hospital NHS Foundation Trust

    RECRUITING

    Papworth Everard, Cambridge, CB23 3RE, United Kingdom

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