About this trial

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 ≥ 70 years with an ICD indication for primary prevention of SCD whether there is an indication for cardiac resynchronization therapy or not.

Eligibility criteria

Qualifiers

≥70 years old,

Left ventricular ejection fraction ≤ 35%, assessed by echocardiography, single-photon emission computed tomography and radionuclide ventriculography and/or cardiac magnetic resonance (CMR) (assessed at inclusion or within the 6 weeks prior to inclusion).

NYHA class II or III

Heart failure HFOT ≥ 3 months (Possible exceptions : possibility of including patients who do not tolerate the maximum dose or who do not tolerate all four therapeutic classes, as well as the possibility of not waiting for three months when one of the classes is discontinued or when dosage adjustments are made due to poor tolerance ...)

Disqualifiers

Enrolled in or planning to enroll in a conflicting interventional trial (trial evaluating the interest of ICD or modifying HFOT outside the last ESC Guidelines)

Prior unstable sustained ventricular arrhythmia requiring external cardioversion

Myocardial infarction within the 40 days

Coronary artery intervention (catheter or surgical) within 90 days

Trial design

Treatments tested in this trial

  • ICD implantation
  • No ICD implantation

Treatment groups

730 Participants
are divided into 2 treatment groups

Locations

19
Centre Hospitalier d'Aix en provence13616, Aix-en-Provence France
CHU Amiens-Picardie-Site sud80054, Amiens France
CHU Brest - Hôpital La Cavale Blanche29200, Brest France
HôpitalHenri Mondor94000, Créteil France

Sponsors and collaborators

Assistance Publique - Hôpitaux de Paris

Lead sponsor

Ministry of Health, France

Collaborator