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Prevention Of Sudden Cardiac Death After Myocardial Infarction by Defibrillator Implantation

Study acronym: PROFID EHRA
StatusRecruiting
PhaseNot applicable
Started2023-11-16
View on ClinicalTrials.gov ↗

Amendment history

The 50 most recent of 79 record versions are listed below. See every version on ClinicalTrials.gov ↗

2026-03-31
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Study titlerevised
Prevention ofOf Sudden Cardiac Death After Myocardial Infarction by Defibrillator Implantation
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Eligibility criteria-31 characters
[...] magnetic resonance imaging [MRI] at least 3 months after MI and at least 3 months prior to enrolment). Signed informed consent. Inclusion criterion I3 defines my [...] n 1 year. Participation in another randomised clinical trial, eitherif withinstudy-specific thetreatment 3is monthsstill prioractive toat enrolment orinto stillPROFID on-goingEHRA. Previous participation in PROFID EHRA. Parallel participat [...]
Secondary endpointsdetails revised at 1 of 5 entries
Study titlerevised
Prevention Ofof Sudden Cardiac Death After Myocardial Infarction by Defibrillator Implantation
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Patients who have survived a myocardial infarction (MI) are at increased risk for sudden cardiac death (SCD) caused by ventricular tachycardia and ventricular fibrillation. A severely reduced left ventricular ejection fraction (LVEF) as a rough overall measure of impaired heart function after MI was shown to indicate a higher risk for SCD. Based on this observation, two landmark randomised trials, MADIT II and SCD-HeFT, were conducted between end of the 1990s and early 2000s. These trials compared the survival of patients with severely reduced LVEF who received an implantable cardioverter-defibrillator with the survival of patients being on medical therapy alone. They reported a significantly better survival of patients in the defibrillator arm and led to international guideline recommendations for routine implantation of defibrillators in survivors of MI with severely impaired LVEF as a means for primary prevention of SCD. Since then, the management of these patients has changed dramatically with the advent of a series of novel drug classes that reduce not only mortality but specifically SCD leading to a substantial decrease of the sudden death rates as well as of the rates of appropriate defibrillator therapies implanted for primary prevention of SCD. At the same time, the complication rates associated with the defibrilllator therapy remain significant without obvious decrease. Thus, the risk-benefit of routine defibrillator implantation for primary prevention of SCD in patients with severely reduced LVEF has substantially changed since the conduction of the landmark trials that established this therapy. Due to the inherent risks and considerable costs of the defibrillator, a novel randomised adequately powered assessment of the potential benefit or harm of the defibrillator in survivors of MI with reduced LVEF under contemporary optimal medical treatment (OMT) appears imperative. OBJECTIVE: To demonstrate that in post-MI patients with symptomatic heart failure who receive OMT for this condition, and with reduced LVEF ≤ 35%, OMT without ICD implantation (index group) is not inferior to OMT with ICD implantation (control group) with respect to all-cause mortality.
Trial Details
NCT Number NCT05665608
Lead Sponsor Charite University, Berlin, Germany
Conditions Sudden Cardiac Death, Myocardial Infarction
Enrollment 3,595 participants
Start Date 2023-11-16
Primary Completion 2027-11-30 (estimated)
Study Completion 2027-11-30 (estimated)
Updated on ClinicalTrials.gov 2026-04-01