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NCT03880708Possibly a fitRecruiting

Registry for inherited dangerous heart rhythm conditions

Ventricular Arrythmia

Part of Genetic & congenital, Heart & circulation clinical trials.

This study is a heart rhythm registry for people with inherited conditions that can cause abnormal heart beats. By collecting health and testing information, researchers hope to better understand these conditions and improve care.

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

Phase
N/A
Enrollment
500 people
Ages
1 hour to 90 years
Study type
Observational

Who can take part

  • You must have been diagnosed with Brugada syndrome, Long QT syndrome, Short QT syndrome, early repolarization syndrome, or CPVT.
  • You should be able to provide basic health information for the registry.
  • You must not already be enrolled in a different clinical trial.

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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