Cardiac MRI Study to Predict Outcomes in Non-dilated Left Ventricular Cardiomyopathy
Using Heart Imaging for Risk Assessment and Better Treatment
Led by Chinese Academy of Medical Sciences, Fuwai Hospital · Updated on 2026-01-21
1000
Participants Needed
1
Research Sites
104 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are examining non-dilated left ventricular cardiomyopathy NDLVC, a subtype of heart muscle disease characterized by abnormalities without enlargement of the left ventricle. This retrospective observational study aims to explore how cardiac magnetic resonance CMR findings relate to long-term outcomes and to identify key risk factors for serious heart-related events in patients with NDLVC. The purpose is to develop a CMR-based risk stratification method to help guide clinical decisions and improve patient care.
Patients diagnosed with NDLVC who underwent CMR at the study institution during the specified period will be enrolled retrospectively. Key CMR parameters analyzed include left ventricular ejection fraction LVEF, late gadolinium enhancement LGE patterns, myocardial strain, and the extent of myocardial fibrosis or fatty replacement. The primary outcome measured is a combination of major adverse cardiac events, such as death, heart transplantation, or left ventricular assist device implantation.
Participant data will be collected from medical records and CMR databases. The study will assess these imaging features against patient outcomes over a follow-up period of up to 100 months. By analyzing these factors, the research aims to clarify the link between specific CMR characteristics and prognosis in NDLVC. This will support better risk assessment and improve clinical management strategies for affected patients.
CONDITIONS
Brief Title
Cardiac Magnetic Resonance for Risk Stratification in Non-dilated Left Ventricular Cardiomyopathy
Research Team
L
Lu Minjie PHD
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Chinese Academy of Medical Sciences, Fuwai Hospital
Lead Sponsor
Who Can Participate
Age: 16Years +
All Genders
Eligibility Criteria
You may qualify if you...
Age 16 years or older
Indexed left ventricular end-diastolic volume below 96 mL/m2 for females and below 105 mL/m2 for males at baseline cardiac magnetic resonance
Left ventricular ejection fraction under 50% and/or presence of non-ischemic left ventricular scar or fatty replacement at baseline cardiac magnetic resonance
You will not qualify if you...
Lack of enhanced cardiac magnetic resonance images due to contraindications like severe kidney disease
Presence of ischemic heart disease defined by major coronary artery stenosis over 50%, ischemic late gadolinium enhancement pattern, or prior coronary revascularization
Moderate to severe valvular heart diseases, congenital heart diseases, or uncontrolled hypertension
Systemic rheumatologic diseases or sarcoidosis
Meeting diagnostic criteria for other cardiomyopathies according to European Society of Cardiology definitions
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Diagnostic Evaluation
Duration - Baseline
Participants undergo cardiac magnetic resonance imaging to assess heart function and structure.
1 visit (in-person)
Long-term Monitoring
Duration - Up to 100 months
Participants are observed over time to assess the occurrence of major cardiac events and overall heart health.
Periodic follow-up visits depending on clinical availability
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Published Research Related To This Trial
CarDiac magnEtic Resonance for prophylactic Implantable cardioVerter defibrillAtor ThErapy in Non-Dilated Left Ventricular Cardiomyopathy: a sub-study from the DERIVATE registry.