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A Study on Early Identification of Myocardial Injury in Wilson Disease Patients Based on Cardiac Magnetic Resonance Multimodal Imaging

A Study on Early Identification of Myocardial Injury in Wilson Disease Patients Based on Cardiac Magnetic Resonance Multimodal Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2026000811
Enrollment
Unknown
Registered
2026-03-30
Start date
2025-01-01
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Wilson Disease

Interventions

Observation group:Wilson disease patient
Control Group:Healthy volunteer

Sponsors

The First Affiliated Hospital of Anhui University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Observation group: 1) Meets the diagnostic criteria for Wilson disease; 2) Age 18-45 years, both sexes; 3) Patients or their families have signed the informed consent form. Control group: 1) Healthy volunteers from the same period; 2) Age 18-45 years, both sexes; 3) Voluntarily participate in this study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: Observation Group: 1) Coexisting active diseases that may significantly impair cardiovascular system function (e.g., severe liver/renal dysfunction, uncontrolled severe infection, thyroid crisis, etc.); 2) Presence of contraindications or high-risk factors for cardiac magnetic resonance (CMR); 3) Poor quality of CMR images; 4) Allergy to the investigational drug; 5) Unable to cooperate to complete the entire trial process. Control Group: 1) Presence of any cardiovascular disease (including hypertension, coronary artery disease, cardiomyopathy, heart failure, arrhythmia, etc.) or other systemic diseases that may affect myocardial structure and function (e.g., Wilson disease, chronic liver disease, chronic kidney disease, diabetes, thyroid dysfunction, etc.); 2) Presence of contraindications or high-risk factors for CMR; 3) Poor quality of CMR images; 4) Allergy to the investigational drug; 5) Unable to cooperate to complete the entire trial process; 6) Pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
End-systolic volume;End-diastolic volume;Stroke volume;Cardiac output;Ejection Fraction;Left ventricular end-systolic volume index;Left ventricular end-diastolic volume index;Content T1 value;Content T2 Value;Extracellular Volume Fraction;

Secondary

MeasureTime frame
High-Sensitivity Troponin I;N-terminal pro-B-type natriuretic peptide;Echocardiogram;12-lead standard electrocardiogram;

Countries

China

Contacts

Public ContactWang Han

The First Affiliated Hospital of Anhui University of Chinese Medicine

neuwhah@126.com0551-62838920

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026