Noninvasive Electrocardiographic Imaging for Individuals at Risk for Apparently Idiopathic Ventricular Fibrillation.
Last updated on July 2021Recruitment
- Recruitment Status
- Enrolling by invitation
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Cardiac Arrest
- Cardiac Arrhythmia
- Cardiovascular Diseases
- Genetic Disease
- Heart Arrest
- Idiopathic Ventricular Fibrillation
- Polymorphic Ventricular Tachycardia
- Sudden Cardiac Death
- Ventricular Arrythmia
- Ventricular Fibrillation
- Design
- Observational Model: CohortTime Perspective: Prospective
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
ECGI combines electrical body-surface mapping with 256 electrodes placed on the thorax with a CT-scan obtaining the anatomy of the heart and torso, hereby able to reconstruct local electrograms, activation and recovery times. In recent research, ECGI provided numerous extra insights into normal card...
ECGI combines electrical body-surface mapping with 256 electrodes placed on the thorax with a CT-scan obtaining the anatomy of the heart and torso, hereby able to reconstruct local electrograms, activation and recovery times. In recent research, ECGI provided numerous extra insights into normal cardiac electrophysiology, but also electrophysiological disorders and disease. The results strongly suggest that ECGI can play a pivotal role in further characterizing arrhythmia mechanisms, therefore could do so for polymorphic VT or idiopathic VF leading to diagnosis and treatment improvement. Moreover, ECGI seems to have the potential to detect arrhythmogenic substrate in individuals before their first event, offering the possibility to diagnose and treat patients before sudden cardiac arrest occurs. In the VIGILANCE study: ECGI will be used to noninvasively characterize the epicardial electrophysiological substrate and triggers of: Patients with unexplained polymorphic VT and VF, Index patients of family cohorts with a specific genetic mutation related to arrhythmogenesis, at high risk for unexplained polymorphic VT and/or VF. Family members, A control cohort. Results will be evaluated for risk stratification. All unexplained polymorphic VT and/or VF patients and their family members will be asked to participate in a National Dutch registry, and these date will be analysed to determine their prognostic value in terms of arrhythmia risk
Tracking Information
- NCT #
- NCT03963271
- Collaborators
- Dutch Heart Foundation
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
- UMC Utrecht
- Investigators
- Principal Investigator: Paul Volders, MD, PhD Maastricht University Medical Centre