Clinical and Genetic Features of Japanese Families with Inherited Arrhythmias: A Multicenter-Registry Study
Not Applicable
Recruiting
- Conditions
- All inherited (familial) arrhythmias, such as congenital or acquired long-QT syndrome, Brugada syndrome, idiopathic VF, PCCD, familial bradicardia syndrome including AF, CPVT, short-QT syndrome, ARVC or other cardiomyopathy (including laminopathy, HCM and DCM).
- Registration Number
- JPRN-UMIN000020593
- Lead Sponsor
- ational Cerebral and Cardioascular Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 3000
Inclusion Criteria
Not provided
Exclusion Criteria
None
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To identify the disease-causing genes and mutations
- Secondary Outcome Measures
Name Time Method Genetic-based personalized medicine