Cardiac Magnetic Resonance Guidance of Implantable Cardioverter Defibrillator Implantation in Non-ischemic Dilated Cardiomyopathy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorProf. Dr. med. Ingo Eitel

About this trial

Patients with diagnostic CMR images for assessment of LGE/fibrosis and evidence/presence of non-ischaemic myocardial fibrosis/scar will be randomized to the following treatment groups in a 1:1 ratio: ICD group or Optimal HF care group.

Eligibility criteria

Qualifiers

NIDCM (idiopathic or familial)*

LVEF ≤35% and presence of fibrosis on CMR

Diagnostic CMR scan

Age ≥18 years

Disqualifiers

ICM [previous myocardial infarction, previous percutaneous coronary intervention]

Other cardiomyopathies (hypertrophic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, restrictive cardiomyopathy, infiltrative cardiomyopathies [e.g. cardiac amyloidosis, cardiac sarcoidosis, hemochromatosis and iron overload cardiomyopathy], left ventricular non-compaction cardiomyopathy, reversible cardiomyopathies [Takotsubo syndrrome, peripartum cardiomyopathy, chemotherapy induced cardiomyopathy].

Myocarditis

Contraindication for CMR at study entry (including severe claustrophobia, pacemaker or ICD, metallic cerebral or intracranial implants, known allergy to gadolinium)

Trial design

Treatments tested in this trial

  • ICD/CRT-D implantation

Treatment groups

760 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Prof. Dr. med. Ingo Eitel

Lead sponsor

University of Luebeck

Sponsor institution

Deutsches Zentrum für Herz-Kreislauf-Forschung (DZHK)

Collaborator