RECRUITING

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

Description

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.

Study Overview

Study Details

Study overview

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.

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

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

Condition
Ventricular Tachycardia
Intervention / Treatment

-

Contacts and Locations

Nashville

Vanderbilt University Medical Center, Nashville, Tennessee, United States, 37232

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Adults aged 18 and older
  • 2. Diagnosed with AF before age 60
  • 3. Scheduled for catheter-based AF ablation (de-novo or repeat)
  • 4. Able to provide written, informed consent
  • 5. P/LP variant in TTN or other CM gene (cases) or identified as a genotype-negative control.
  • 1. Diagnosed with a genetic CM or arrhythmia syndrome prior to AF
  • 2. VUS in 'possibly pathogenic' subgroup (control group only)
  • 3. Pacemaker or ICD
  • 4. Previous PVC or VT ablation
  • 5. LVEF \<20%
  • 6. Prosthetic mitral or aortic valve
  • 7. Contraindication to heparin
  • 8. Prior myocardial infarction.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Vanderbilt University Medical Center,

Moore B Shoemaker, MD, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center

Study Record Dates

2027-01-01