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Multicenter Cohort Study on the Deep Phenotyping of Dilated Cardiomyopathy Based on Multimodal Data

Multicenter Cohort Study on the Deep Phenotyping of Dilated Cardiomyopathy Based on Multimodal Data

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086440
Enrollment
Unknown
Registered
2024-07-02
Start date
2024-07-02
Completion date
Unknown
Last updated
2024-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dilated cardiomyopathy

Interventions

NA:NA

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: The diagnostic criteria for dilated cardiomyopathy are based on the Chinese Guidelines for the Diagnosis and Treatment of Dilated Cardiomyopathy. Age = 18 years old, completed baseline cardiac magnetic resonance imaging, CMR results meet the diagnostic criteria of DCM, that is, left ventricular end diastolic diameter (LVEDD)>55mm (male) and>50mm (female) with LVEF<45%, signed an informed consent form

Exclusion criteria

Exclusion criteria: 1. Secondary hypertension, hypertensive emergencies; 2. Concomitant coronary heart disease and ischemic cardiomyopathy; 3. Myocarditis; 4. Merge autoimmune diseases; 5. Merge with other structural heart diseases, such as valve disease, congenital heart disease, etc; 6. Received pacemaker treatment; 7. Severe pulmonary diseases, pulmonary heart disease; 8. Concomitant severe liver and kidney dysfunction; 9. Severe claustrophobia and other intolerable cardiac magnetic resonance imaging examinations; 10. Refusal to participate in the research of this project or failure to sign an informed consent form.

Design outcomes

Primary

MeasureTime frame
Clinical information collection;Magnetic resonance imaging acquisition;

Countries

China

Contacts

Public ContactChen Yucheng

West China Hospital of Sichuan University

chenyucheng2003@126.com+86 189 8060 2149

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026