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Prospective Phenotyping for Genetic Subtypes of Early-onset Atrial Fibrillation
Sponsor: Vanderbilt University Medical Center
Summary
This is a prospective, case-control study that seeks to learn about the role of genetics in early onset atrial fibrillation (AF) and if genetic testing can be used to improve how the investigators treat atrial fibrillation. The study will enroll 225 participants. Eligible participants will have undergone sequencing for arrhythmia and cardiomyopathy (CM) genes. Based on those results, participants will be recruited for an outpatient research visit with testing that includes cardiac MRI, rest/stress/signal-averaged ECGs, and cardiac monitoring. If an inherited arrhythmia/CM syndrome is diagnosed, guideline-directed changes to medical care will be recommended.
Key Details
Gender
All
Age Range
15 Years - Any
Study Type
OBSERVATIONAL
Enrollment
225
Start Date
2022-04-27
Completion Date
2026-10
Last Updated
2025-05-11
Healthy Volunteers
Not specified
Conditions
Interventions
None/Observational Studies
This is an observational study and there is no intervention.
Locations (1)
Vanderbilt University Medical Center
Nashville, Tennessee, United States