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ElectroPhySiological Characterization Of the Arrhythmia Substrate for Sudden Cardiac Death PrEdiction

NCT07020702 — Not applicable, Recruiting, 210 participants, University Hospital, Bordeaux

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RegistryNCT07020702, acronym EP-SCOPE
StatusRecruiting
PhaseNot applicable
Study typeInterventional; non randomized, parallel, masking: none, prevention
Enrollment210 (Estimated)
SponsorUniversity Hospital, Bordeaux (Other)
ConditionsVentricular Arrhythmia, Cardiomyopathies, Left Ventricular Ejection Fraction Less Then or Equal to 50percent
InterventionsImplantation of an ICD (Device)
Datesstart 2023-06-12, primary completion 2030-09-12 (estimated), completion 2030-09-12 (estimated), first posted 2025-06-13, last updated 2025-07-10
Locations3 sites in France

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-Summary

EP-SCOPE is a prospective, multicentric, non-randomized pilot study that aims to estimate the risk of life-threatening ventricular arrhythmia through use of advanced electrophysiological studies in patients with ischemic or non-ischemic cardiomyopathy with left ventricular ejection fraction (LVEF) <50% and risk factors of ventricular arrhythmia, otherwise not considered for implantation of an implantable cardioverter defibrillator (ICD).

The objective is to assess the effectiveness of a risk stratification strategy based on detailed electrophysiological exploration of the left ventricle and programmed ventricular stimulation.

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+Detailed description

Responsible for 10% of deaths in the general population, sudden cardiac death is mostly caused by malignant ventricular arrhythmias (80%). These arrhythmias mainly occur in cardiomyopathies (75-90%). Currently, the prevention of sudden death is based on risk stratification according to the evaluation of myocardial contractility with indications for prophylactic ICD implantation reserved for LVEF ≤ 35%. This predictor is notoriously insufficient for several main reasons: 1) While ICDs are indicated in patients with LVEF ≤35%, only a minority (2 -5% per year) will suffer from arrhythmia and therefore benefits from ICD implantation, while all will be subject to potential complications. 2) The majority of sudden death (70-80%) occur in patients with LVEF >35%; while they have a lower arrhythmia risk (1-2% per year), they constitute a population four times larger, which is not stratified. 3) Finally, the cardiomyopathy population is broad, and include distinct clinical scenarios that are not specifically addressed.

While conventional electrophysiological studies only boast a limited number of measurements, the proposed strategy is a detailed electrophysiological characterization of the altered ventricle. Measurements include a detailed mapping of the left ventricle in the basal state and during extrastimuli, and programmed stimulation of the right and left ventricle including the simultaneous recording of the Purkinje system.

Follow-up will be performed for 3 years, looking for the occurrence of major arrhythmic events such as: 1) Appropriate therapy (for VT/VF) delivered by an ICD or 2) documented ventricular arrhythmia on ECG, implantable loop recorder or pacemaker or 3) Clinical sudden death.

+Arms and interventions

ArmTypeInterventionsDescription
Implantation of an ICDExperimentalDevice: Implantation of an ICDPatients implanted with an ICD
Clinical follow-upNo interventionPatients not implanted with an ICD
  • Implantation of an ICD (Device): Implantation of an ICD

+Outcome measures

Primary outcomes

  • Occurrence of major rhythmic events [60 months]: Follow-up on Occurrence of major rhythmic events

Secondary outcomes

  • Surfaces distributions of abnormal ventricular potentials [Day 1]
  • Spatial distributions of abnormal ventricular potentials [Day 1]
  • Purkinje potentials in induced arrhythmias [Day 1]: Presence or absence

+Eligibility

Sex: All, ages: 18 Years to 80 Years

Inclusion Criteria:

* Patient with cardiomyopathy with 35%<LVEF<50% and at least one risk factor
* Patients with cardiomyopathy with LVEF≤35% and an indication for cardiac resynchronisation

Exclusion Criteria:

* Patients who are minors or aged 80 or over
* Patients with unstable coronary artery disease
* Myocardial infarction less than 40 days old
* Coronary revascularisation <90 days
* Patients with intracardiac thrombus
* Patients with a mechanical heart valve
* Patient implanted with an automatic defibrillator
* Patient life expectancy <1 year
* Pregnant or breast-feeding women
* Anti-arrhythmic drugs other than beta-blockers and amiodarone

+Locations (3)

FacilityCityCountryStatus
CHU de Clermont-FerrandClermont-FerrandFranceRecruiting
CHU de Bordeaux - Hôpital Cardiologique du Haut-LévêquePessacFranceRecruiting
CHU de Saint-EtienneSaint-EtienneFranceRecruiting

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