Clin2
NCT07849738Possibly a fitRecruiting

Genetic testing after sudden cardiac death

Tachycardia

Part of Heart & circulation clinical trials.

This study looks at the DNA of young people who died suddenly without a clear cause, to find inherited heart conditions. If a genetic cause is found, close family members can be tested to learn their own risk and get preventive care.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
200 people
Ages
5 years to 50 years
Study type
Observational

Who can take part

  • Passed away suddenly and unexpectedly between ages 1 and 50
  • Death was not due to injury or poisoning
  • An autopsy was done at the Death Verification Service in São Paulo
  • A family member gives permission to use the deceased person's samples
  • For relatives: a close family member (parent, sibling, or child) must have a confirmed genetic heart condition

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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