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Helium-free Magnetocardiography Guided Therapy for Stable Coronary Artery Disease — A Randomized Controlled Trial

Helium-free Magnetocardiography Guided Therapy for Stable Coronary Artery Disease — A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126740
Enrollment
Unknown
Registered
2026-06-15
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Stable Coronary Artery Disease

Interventions

Conventional Management Group:Treatment strategies were recommended based on stenosis severity, pre-test probability, and functional test results: For patients with 50-70% stenosis, if the pre-test pr
if the pre-test probability was =15%, it was advised to recommend treatment strategies considering functional test results. For patients with CCTA-indicated 70-90% stenosis, clinicians could directly
MCG Group:Based on MCG results, either ICA or optimal medical therapy was recommended.

Sponsors

Beijing Anzhen Hosptial, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18–80 years, both genders; 2. Patients with stable coronary artery disease (CAD); 3. CCTA indicates at least one major epicardial vessel (vessel diameter >=2.5 mm) with 50–90% stenosis. Patients with 50–69% stenosis must have typical or atypical angina pectoris, while patients with 70–90% stenosis are not restricted by the presence of chest pain symptoms. *Note: The three characteristics of chest pain are: (1) chest discomfort lasting less than 15 minutes; (2) induced by physical activity or emotional stress; (3) relieved by rest or nitrates. Typical angina pectoris: all three characteristics present; atypical angina pectoris: two characteristics present; non-anginal chest pain: =1 characteristic present.* 4. Willing to participate voluntarily in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Previous myocardial infarction, PCI, CABG, or coronary angiography indicating stenosis >=50% in a major vessel. 2. CCTA indicating left main coronary artery stenosis >50% and/or three-vessel disease. 3. History of cardiac dysfunction (>= NYHA Class III), severe congenital heart disease, valvular heart disease, or cardiomyopathy. 4. Complex arrhythmias, such as frequent atrial premature beats, ventricular premature beats, atrial fibrillation, atrial flutter, etc. 5. History of metal implant placement (including mechanical valves, pacemakers, orthopedic internal fixation plates, drug pumps, etc.). 6. Claustrophobia. 7. Severe thoracic deformity. 8. Active bleeding. 9. Any disease with an expected survival of less than 1 year. 10. Completion of any of the following tests prior to enrollment: exercise ECG, stress echocardiography, stress SPECT, or stress CMR. 11. Any other condition where the investigator considers the patient unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
Proportion of patients with non-obstructive coronary artery disease on invasive coronary angiography (ICA) within 90 days. :;

Secondary

MeasureTime frame
Major Adverse Cardiovascular Events;Seattle Angina Questionnaire;Total medical expenditure of patients in the study;

Countries

China

Contacts

Public ContactSong Xiantao

Beijing Anzhen Hosptial, Capital Medical University

tcc2033@163.com+86 152 0164 8899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026