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Cardioverter DefIbriIlator PlacEMent for priMary Prevention of Sudden cArdiac Death in Patients Older Than 75 Years

Cardioverter DefIbriIlator PlacEMent for priMary Prevention of Sudden cArdiac Death in Patients Older Than 75 Years

Recruiting
75 years and older
All
Phase N/A

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Overview

The primary objective of DILEMMA study is to assess whether the "heart failure optimal therapy alone (HFOT)" strategy is non inferior to the "HFOT+ICD" strategy in terms of overall survival 48 months after randomization, in patients ≥ 75 years with an ICD indication for primary prevention of SCD whether there is an indication for cardiac resynchronization therapy or not.

Description

Rationale Although not recognized by guidelines, there is no available data demonstrating the benefit of Implantable Cardioverter Defibrillator (ICD) for primary prevention strategy of Sudden Cardiac Death (SCD) in elderly. Nevertheless, ICD are currently implanted in this population by extending the results obtained in randomized trials involving younger subjects to the elderly. Finally, if the absence of implantation in the elderly was not inferior to the implantation of such a device, the non-implantation would avoid the device-related complications and decrease the health costs.

Main objective The primary objective of DILEMMA study is to assess whether the "heart failure optimal therapy alone (HFOT)" strategy is non inferior to the "HFOT+ICD" strategy in terms of overall survival 48 months after randomization, in patients ≥ 75 years with an ICD indication for primary prevention of SCD whether there is an indication for cardiac resynchronization therapy or not.

Design This is a 2-arm parallel non-inferiority, randomized, open label, multicenter trial. 730 patients will be included over 4 years. Follow up will last 4 years.

Eligibility

Inclusion Criteria:

  • ≥75 years old,
  • Left ventricular ejection fraction ≤ 35%
  • NYHA class II or III
  • Heart failure HFOT ≥ 3 months
  • Providing informed consent
  • Affiliated to a French Health Insurance system.

Exclusion Criteria:

  • Enrolled in or planning to enroll in a conflicting interventional trial
  • Prior unstable sustained ventricular arrhythmia requiring external cardioversion
  • Myocardial infarction within the 40 days
  • Coronary artery intervention (catheter or surgical) within 90 days
  • History of syncope in the previous 6 months
  • Advanced cerebrovascular disease
  • Cognitive impairment leading to the incapacity of consent
  • Any disease other than cardiac disease (e.g. cancer, uremia, liver failure), associated with a likelihood of survival less than 1 year.
  • Patient under tutorship, curatorship, or legal safeguard
  • Persons deprived of their liberty by judicial or administrative decision (prisoner)

Study details
    Heart Failure
    Primary Prevention of Sudden Cardiac Death
    Implantable Cardioverter Defibrillator

NCT05373940

Assistance Publique - Hôpitaux de Paris

26 January 2024

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