RecruitingNCT06647459

Defining the Risk of Ventricular Tachycardia in Genetic Forms of Early-onset Atrial Fibrillation

Defining the Risk of Ventricular Tachycardia in Genetic Forms of Early-onset Atrial


Sponsor

Vanderbilt University Medical Center

Enrollment

200 participants

Start Date

Dec 13, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

To use programmed ventricular stimulation at the time of AF ablation to define the prevalence and mechanism of inducible ventricular tachycardia (VT); pace-mapping to define the site of origin of ventricular arrhythmias; and voltage mapping to define low voltage scar substrate in the basal LV in patients with pathogenic TTN variants compared to genotype-negative controls.


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • Adults aged 18 and older
  • Diagnosed with AF before age 60
  • Scheduled for catheter-based AF ablation (de-novo or repeat)
  • Able to provide written, informed consent
  • P/LP variant in TTN or other CM gene (cases) or identified as a genotype-negative control.

Exclusion Criteria8

  • Diagnosed with a genetic CM or arrhythmia syndrome prior to AF
  • VUS in 'possibly pathogenic' subgroup (control group only)
  • Pacemaker or ICD
  • Previous PVC or VT ablation
  • LVEF \<20%
  • Prosthetic mitral or aortic valve
  • Contraindication to heparin
  • Prior myocardial infarction.

Interventions

DIAGNOSTIC_TESTEP Study

To use programmed ventricular stimulation at the time of AF ablation to define the prevalence and mechanism of inducible ventricular tachycardia (VT); pace-mapping to define the site of origin of ventricular arrhythmias; and voltage mapping to define low voltage scar substrate in the basal LV in patients with pathogenic TTN variants compared to genotype-negative controls.


Locations(1)

Vanderbilt University Medical Center

Nashville, Tennessee, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06647459


Related Trials