MCG for Non-Obstructive Myocardial Ischemia
Magnetocardiography in the Identification of Non-Obstructive Myocardial Ischemia of Patients With Acute Chest Pain
1 other identifier
observational
3,786
1 country
1
Brief Summary
The aim of this prospective study is to identify Non-Obstructive Myocardial Ischemia of patients who have acute chest pain using Magnetocardiography.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 15, 2025
CompletedFirst Submitted
Initial submission to the registry
June 14, 2026
CompletedFirst Posted
Study publicly available on registry
June 18, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2026
ExpectedJune 24, 2026
June 1, 2026
1.2 years
June 14, 2026
June 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Efficacy of MCG for the detection of Non-Obstructive Myocardial Ischemia
Establishing an algorithm model of MCG in identifying Non-Obstructive Myocardial Ischemia, the efficacy of the model was assessed by sensitivity, specificity
from the date of enrollment until the date of discharge, up to 30 days]
Interventions
Assessing the performance of magnetocardiography device for detecting non-obstructive myocardial ischemia using ultrasound coronary flow reserve (CFR) as the reference standard.
Eligibility Criteria
patient who suffers from cardiogenic chest pain suspected with Non-Obstructive Myocardial Ischemia
You may qualify if:
- Age 18 years or older;
- Patients with symptoms of myocardial ischemia such as angina pectoris, who have CAG showing \<70% stenosis at the most severe site or CTA showing non-severe stenosis
- Signed informed consent.
You may not qualify if:
- Patients with absolute or relative contraindications to CFR-loaded myocardial perfusion, including acute myocardial infarction within 48 hours, significant left main coronary artery stenosis, bronchial asthma, and adenosine injection allergy;
- Patients with Non-ischemic dilated cardiomyopathy, or hypertrophic cardiomyopathy, or moderate or severe valvular disease;
- Patients with Hemodynamic instability (systolic blood pressure\<90 mmHg, or who requires vasoactive drugs), or patients with tachyarrhythmia,
- #degree atrioventricular block and above that have not returned to normal;
- Patients who have severe renal abnormality with eGFR \<30 ml/min, or patients who are on dialysis;
- Patients with malignant tumors with predicted survival of less than 1 year;
- Pregnant or breastfeeding women;
- Patients who are unable to enter the MCG device, who are unable to perform MCG examination due to interference from metal implants or other reasons, or who are deemed by the investigators to be unsuitable for enrollment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Qliu Hospital of Shandong University
Jinan, Shandong, 250012, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yuguo Chen, Professor
Qliu Hospital of Shandong University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 14, 2026
First Posted
June 18, 2026
Study Start
April 15, 2025
Primary Completion
June 30, 2026
Study Completion (Estimated)
August 30, 2026
Last Updated
June 24, 2026
Record last verified: 2026-06