Could your genes make you prone to broken heart syndrome?

NCT ID NCT04513054

Recruiting now Knowledge-focused Sponsor: University of Aberdeen Source: ClinicalTrials.gov ↗

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

Summary

This study aims to find out if genetics play a role in who gets broken heart syndrome (Takotsubo cardiomyopathy), a condition that mimics a heart attack and is often triggered by intense stress. Researchers will collect blood samples from 700 people diagnosed with the condition in Scotland and analyze their DNA. The goal is to identify genetic variations that may increase susceptibility, which could also have implications for family members.

What this could mean

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

What this could lead to: If successful, this could help identify people at higher risk for broken heart syndrome and possibly inform future screening or prevention strategies.
What could go wrong: This is an observational genetic study, not a treatment trial. It may not find clear genetic links, and any findings would need years of further research before practical use.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

Tako-tsubo cardiomyopathy

As listed by the trial registrant

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

TAKOTSUBO CARDIOMYOPATHY

Contacts and locations

Locations

Cardiac Research Office, Aberdeen Royal Infirmary
RECRUITING

Aberdeen, Aberdeenshire, AB25 2ZD, United Kingdom
Cardiovascular Research Facility
RECRUITING

Aberdeen, Aberdeenshire, AB25 2ZD, United Kingdom

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