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NCT06575881Recruiting

Defining the Risk of Ventricular Tachycardia in Genetic Cardiomyopathies

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

Source: ClinicalTrials.gov · Last updated 6 May 2026

Brief summary (registry, in English)

The goal of this observational study is to determine if electrophysiologic mapping and cardiac MRI can help identify patients that have genetic forms of cardiomyopathy that are at high risk for development of dangerous ventricular arrhythmias. The investigators aim to study: 1. the prevalence and mechanism of inducible ventricular tachycardia 2. pace-mapping to define the site of origin of ventricular arrhythmias 3. voltage mapping to define low voltage scar substrate in the basal LV to determine the risk of development of ventricular arrhythmias in patients with genetic forms of cardiomyopathy. Participants will undergo cardiac MRI before their scheduled procedure and voltage mapping during their scheduled procedure as part of data collection.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
26 Aug 2024
Start date
13 Dec 2023
Primary completion date
Dec 2028
Lead sponsor
Vanderbilt University Medical Center
NCT number
NCT06575881

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 13 Dec 2023 to the primary completion date, Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Diagnosed with a genetic CM or arrhythmia syndrome prior to ablation procedure
  • Previous PVC or VT ablation
  • Prior myocardial infarction

Lab values

  • LVEF \<20%

Other

  • VUS in 'possibly pathogenic' subgroup (control group only)
  • Prosthetic mitral or aortic valve
  • Contraindication to heparin

Who the study is looking for

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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Vanderbilt University Medical Center
Coordinator of this site? Confirm its status
NashvilleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.