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Clinical Trial ● Currently Recruiting Non-phase study NCT05665608

Prevention Of Sudden Cardiac Death After Myocardial Infarction by Defibrillator Implantation

Prevention Of Sudden Cardiac Death After Myocardial Infarction by Defibrillator Implantation — Recruiting • Non-phase study • Cardiology / Cardiovascular • NCT05665608.

📅 01 Apr 2026 ⏱ 3 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Non-phase study
NCT ID
NCT05665608
Sponsor
Charite University, Berlin, Germany
Start
2023-11-16
ClinicaliQ Trial Snapshot
  • Prevention Of Sudden Cardiac Death After Myocardial Infarction by Defibrillator Implantation — Recruiting • Non-phase study • Cardiology / Cardiovascular • NCT05665608.
  • 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….
  • Sponsor: Charite University, Berlin, Germany.

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What This Trial Is Studying

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…

Eligibility Snapshot
  • : 1. Age ≥18 years. 2. Naïve to implantation of any pacemaker or defibrillator 3. Documented history of MI either as ST segment elevation myocardial infarction (STEMI) or as non-ST segment elevation myocardial infarction (NSTEMI) at least 3 months prior to enrolment. 4. Symptomatic heart failure with New York Heart Association (NYHA) class II or III. 5. On OMT for at least 3 months prior to enrolment. 6. LVEF ≤ 35% (at transthoracic echocardiography or cardiac magnetic resonance imaging [MRI] at least 3 months after MI). 7. Signed informed consent. Inclusion criterion I3 defines myocardial infarction according to the 2018 ESC/ACC/AHA/WHF Fourth Universal Definition of myocardial infarction

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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