Registry for inherited ventricular arrhythmias in China

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational, prospective, multi-center registry aims to build a risk stratification for malignant inherited ventricular arrhythmias, including conditions like Brugada syndrome and Long QT syndrome. The study will recruit 500 participants from 10 centers across China, collecting clinical data from medical records and blood samples for genetic analysis. Participants will be followed up every six months to monitor their condition and treatment outcomes. The goal is to explore the correlation between genotype and phenotype to aid in molecular diagnosis and risk stratification.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* diagnosed as Brugada syndrome(Brs)、Long QT syndrome(LQTS)、Short QT syndrome(SQTS)、Early repolarization syndrome(ERS) or Catecholaminergic polymorphic ventricular tachycardia(CPVT).

Exclusion Criteria:

* patients were enrolled by other clinical trials.

Where it's running

• China National Center for Cardiovascular Diseases
  Beijing, Beijing Municipality, China Recruiting

Study contacts

• Study coordinator: Yan YAO, MD,PhD
• Email: ianyao@263.net.cn
• Phone: +86-13901121319

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.