Clinical trial Recruiting at 1 site Observational Ages 18 to 80

Heart MRI scar analysis to predict sudden cardiac death after a heart attack

Official title: Comprehensive Cardiac Magnetic Resonance Imaging Evaluation of Myocardial Scar for Predicting Sudden Cardiac Death Post Myocardial Infarction

Run by Beijing Anzhen Hospital · NCT07137936 · Data updated 2026-11-12

This study will see if detailed heart MRI scar pictures can predict out-of-hospital sudden cardiac death in people who have had a heart attack.

More Myocardial Infarction (MI) trials

Quick facts

Study typeObservational
Ages18 Years to 80 Years
SexAll
Enrollment1000 (estimated)
SponsorBeijing Anzhen Hospital
Academic / other
Locations1 site (Beijing)
StatusRecruiting
StartedJanuary 1, 2026
Main results expectedDecember 31, 2036
Study endsDecember 31, 2036
Registry record updatedAugust 22, 2025
Trial IDNCT07137936 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–80 who had a heart attack and completed a cardiac MRI at least one month later at Beijing Anzhen Hospital are the intended participants.

Probably not a fit

Patients who already have an ICD, have known primary arrhythmia syndromes, established non‑ischemic cardiomyopathy, significant valvular disease, or a life expectancy under one year are unlikely to benefit from the study findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This ambispective observational cohort uses cardiac magnetic resonance (CMR) scar imaging, especially late gadolinium enhancement, to link scar characteristics with post‑MI sudden cardiac death. Phase 1 retrospectively enrolled patients treated for MI from 2015–2025 who had CMR at least one month after their MI and collected baseline clinical and imaging data. Phase 2 continues prospective follow-up from 2026–2036 with clinic visits and telephone check‑ins every six months to capture outcomes. The goal is to combine imaging and clinical data into a validated multimodal risk score to better identify high‑risk patients.

Why it matters

Potential benefit: If successful, the work could help clinicians identify post‑MI patients at higher risk of sudden cardiac death so preventive treatments like ICDs can be targeted more accurately.

How similar studies have gone: Previous studies have suggested that CMR scar measures (LGE) relate to arrhythmic risk, but larger validated multimodal risk scores remain limited and need further confirmation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age between 18 and 80 years.
2. Completion of cardiac magnetic resonance (CMR) imaging at Anzhen Hospital during the stable phase (≥1 month) following an acute myocardial infarction (MI).

Exclusion Criteria:

1. Prior implantation of an implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy defibrillator (CRT-D) before the index MI.
2. Pre-existing diagnosis of a primary arrhythmia syndrome (e.g., long QT syndrome, Brugada syndrome) before the index MI.
3. Concurrent end-stage disease (e.g., advanced malignancy) directly resulting in an estimated life expectancy of less than one year.
4. History of established non-ischemic cardiomyopathy (e.g., dilated, hypertrophic, or restrictive cardiomyopathy) before the index MI.
5. Significant concomitant valvular heart disease. Status post mechanical heart valve replacement.
6. Patients refuse to be followed up.

Where it's running

  • Beijing Anzhen Hospital
    Beijing, China
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.