Ultra-sensitive Magnetocardiography in the Accurate Identification of Severe Coronary Lesions and Myocardial Necrosis

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Magnetocardiography (MCG) is a promising noninvasive and accurate method for detecting myocardial ischemia. Although progress has been made in this area, there is a lack of studies using up-to-date examination instruments for the calibration of MCG analysis. This is a prospective single-center study aiming to build accurate analytical models of MCG to detect coronary lesions and myocardial necrosis. Coronary lesions are measured by coronary angiography (CAG) or coronary CTA, and are defined by both the stenosis degree and the computer-simulated fraction flow reserve. Myocardial necrosis is examined and quantified by cardiac MR. Healthy volunteers, chest pain patients who will receive CAG or CTA examination, and patients with acute myocardial infarction will be enrolled in this study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 79
Healthy Volunteers: t
View:

• Age 18-79 years old;

• No history of cardiovascular disease (coronary heart disease, structural heart disease, arrhythmia, heart failure, stroke, pulmonary embolism, aortic dissection, etc.), no cardiovascular risk factors (hypertension, diabetes, hyperlipidemia). For people over 65 years old, those with hypertension or hyperlipidemia, but with well-controlled blood pressure and lipid levels, taking no more than 2 drugs, and echocardiography showing no left ventricular hypertrophy, can be included;

• The electrocardiogram is normal, and the cardiac ultrasound is basically normal in the past 1 year (mild valvular regurgitation can be included).

• Sign the informed consent.

• Age 18-79 years old;

• Those with chest pain symptoms, diagnosed or highly suspected by the attending doctor or above as stable angina pectoris (SA), unstable angina pectoris (UA), non-ST segment elevation myocardial infarction (NSTEMI), ST segment elevation myocardial infarction (STEMI), and plan to receive CAG or coronary CTA;

• Sign the informed consent.

• Age 18-79 years old;

• The attending doctor or above has diagnosed the patient as acute myocardial infarction (NSTEMI, STEMI), the condition of whom is relatively stable, and CMR examination is feasible after evaluation.

• Sign the informed consent.

Locations
Other Locations
China
Qilu Hospital of Shandong University
RECRUITING
Jinan
Contact Information
Primary
Jiaojiao Pang, Dr.
jiaojiaopang@126.com
0086-0531-82165674
Time Frame
Start Date: 2022-05-30
Estimated Completion Date: 2024-12-30
Participants
Target number of participants: 430
Treatments
Other: healthy volunteers
Experimental: Chest pain patients who will undergo CAG or CTA
Experimental: AMI patients
Sponsors
Collaborators: Second Affiliated Hospital, School of Medicine, Zhejiang University, Jining First People's Hospital, Weifang People's Hospital, First Affiliated Hospital Xi'an Jiaotong University, First People's Hospital of Hangzhou, The First Affiliated Hospital with Nanjing Medical University, Qianfoshan Hospital, Guangdong Provincial Hospital of Traditional Chinese Medicine, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, Chongqing Emergency Medical Center, Heze Municipal Hospital, Linyi People's Hospital, Weihai Central Hospital
Leads: Qilu Hospital of Shandong University

This content was sourced from clinicaltrials.gov