Atrial Fibrillation Clinical Trial
Official title:
Esophageal 3D Mapping System for Cardiac Arrhythmias: Pilot Study to Establish Basis for Improved Arrhythmia Diagnostics Using the esoECG-3D Catheter
The aim of the study is to develop and validate a novel esophageal mapping system to improve the diagnostics of cardiac arrhythmias. Using a newly designed esophageal ECG catheter, esophageal ECGs (eECGs) will be recorded in 40 patients during an electrophysiological (EP) study and/or ablation procedure and in 12 healthy volunteers. In parallel acquired intracardiac electrograms will serve as reference for the developed mapping systems accuracy. Additionally, the esophageal mapping system will be compared to that of the standard 12-lead surface ECG in regard to its diagnostic performance.
Background
Cardiac arrhythmias are common and may have devastating consequences for affected patients.
To prevent f.e. strokes due to atrial fibrillation, heart failures as a consequence of
long-standing tachyarrhythmias or death due to ventricular fibrillation, accurate and timely
diagnoses are essential. The standard diagnostic tool for heart rhythm disorders in everyday
clinical life is the 12-channel surface electrocardiogram (ECG). However, despite its
strengths, the surface ECG suffers from several limitations. Especially on the
supraventricular level, the low atrial signal amplitude renders it prone to errors and causes
surface ECGs to quickly reach the limits of their diagnostic capacities.
This limitation could be overcome by recordings through the esophagus. Owing the close
anatomical relationship, esophageal ECGs have an excellent atrial signal quality. To fully
exploit their potential, a novel esophageal ECG catheter (esoECG catheter) with 3-dimensional
electrode arrangement was developed. The aim of this study is to use the esoECG-3D catheter
to develop and validate a non-invasive esophageal mapping system in order to improve the
diagnostics of cardiac arrhythmias and consequently the therapy of patients suffering from
these disorders.
Objectives
Primary objective (A1): Development of an esophageal non-invasive mapping system which shall
be able to depict
- A1.1: the source of focal triggers
- A1.2: the sequence of cardiac depolarization
with high spatial and temporal resolution.
Secondary objectives (A2):
- A2.1: outperform the diagnostic accuracy of 12-lead ECGs in bedside arrhythmia
diagnostics
- A2.2: estimate the speed of myocardial depolarization on the left atrial wall from
esophageal ECG tracings
- A2.3: extract respiration signals from esophageal ECG tracings
- A2.4: determine the wearing comfort of the device
- A2.5: determine the operability of the device
Safety objective (A3): Determination of safety of the esoECG-3D catheter for esophageal ECG
recordings with respect to:
- A3.1: device related adverse events
- A3.2: device related serious adverse events
- A3.3: device failures, including insertion failure
Methods
Esophageal ECGs will be acquired from a total of 52 participants using the esophageal
esoECG-3D catheter. 40 of these will be recorded during an electrophysiological study and/or
ablation procedure to obtain a reference (intracardiac measurements) for the evaluation of
outcome measures. In a subset of patients, defined pacing maneuvers will be performed;
12-channel ECG and breathing sensor recordings will be obtained from all participants in
parallel to eECG measurements. The acquired data will be used for development of algorithms
to non-invasively map the hearts depolarization process from recordings in the esophagus.
Outcome evaluation will be performed after completion of all measurements and after
implementation of the final mapping algorithms.
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