Arrhythmia Clinical Trial
Official title:
The EU TrigTreat Clinical Study: An Advanced Diagnostics and Observational Trial for Arrhythmia Risk Stratification and Correlation With Genotype
The prospective EUTrigTreat multi-center study is an observational, advanced diagnostics and
genetic risk stratification trial in patients with standard indications for ICD treatment,
with and without myocardial infarction in their history.
Its aims are fourfold: 1) To accurately risk stratify a large cohort of implantable
cardioverter-defibrillator (ICD) patients for ICD shock risk and mortality using traditional
risk markers as well as genetic markers 2) To find a link between repolarization biomarkers
and genetic markers of calcium metabolism. 3) To compare invasive and noninvasive
electrophysiologic (EP) testing systematically 4) To assess temporal changes of typical
noninvasive risk stratifiers and their prognostic implication.
In five European academic clinical centers, 700 ICD patients are prospectively enrolled
(optionally the number of enrolled patients may be expanded to 1000 patients). Comprehensive
non-invasive risk stratifying ECG diagnostics including beat-to-beat variability of
repolarization (BVR) are applied, and candidate genes associated with malignant arrhythmias
are analyzed. Programmed electrical stimulation is performed to test for inducibility of
malignant ventricular arrhythmias and BVR. In a subset of patients, electrophysiologic
studies include recording of monophasic action potentials (MAP) from the right ventricle for
assessment of restitution properties. Non-invasive risk stratifying ECG methods are repeated
annually. Outcome (mortality, ICD shocks) will be assessed until September 2014.
An increasing number of patients receive implantable cardioverter-defibrillators for primary
and secondary prevention of sudden cardiac death. Within this group, it is difficult to
differentiate between patients at high risk with need for additional treatment and, on the
other hand, patients at low risk without benefit from implantable cardioverter-defibrillator
therapy. Risk stratification techniques have been studied extensively over the last decades,
but no conclusive recommendations can be found in the current guidelines for prevention of
SCD. Furthermore, new genetic markers associated with sudden cardiac death were discovered
recently, however, have not been implemented in concurrent risk analysis. Last, time
dependent changes of risk stratification assessment are unknown.
The prospective EUTrigTreat multi-center study is an observational, advanced diagnostics and
genetic risk stratification trial in patients with standard indications for ICD treatment
and without myocardial infarction in their history.
Its aims are fourfold: 1) To accurately risk stratify a large cohort of implantable
cardioverter-defibrillator (ICD) patients for ICD shock risk and mortality using traditional
risk markers as well as genetic markers 2) To find a link between repolarization biomarkers
and genetic markers of calcium metabolism. 3) To compare invasive and noninvasive
electrophysiologic (EP) testing systematically 4) To assess temporal changes of typical
noninvasive risk stratifiers and their prognostic implication.
In four European academic clinical centers, 700 ICD patients are prospectively enrolled.
Optionally, the number of patients may be expanded to 1000. Comprehensive non-invasive risk
stratifying ECG diagnostics including beat-to-beat variability of repolarization (BVR) are
applied, and candidate genes associated with malignant arrhythmias are analyzed. Programmed
electrical stimulation is performed to test for inducibility of malignant ventricular
arrhythmias and BVR. In a subset of patients, electrophysiologic studies include recording
of monophasic action potentials (MAP) from the right ventricle for assessment of restitution
properties. Non-invasive risk stratifying ECG methods are repeated annually. Outcome
(mortality, ICD shocks) will be assessed until September 2014.
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Observational Model: Cohort, Time Perspective: Prospective
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