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A Disease-Specific Cohort Study on the Application of High-Frequency QRS Detection Technology in Chest Pain Patients

A Disease-Specific Cohort Study on the Application of High-Frequency QRS Detection Technology in Chest Pain Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111570
Enrollment
Unknown
Registered
2025-11-03
Start date
2025-11-03
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Cardiovascular Disease

Interventions

Oobservational group:None

Sponsors

Hunan Provincial People's Hospital (The First Affiliated Hospital of Hunan Normal University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Participants are Chinese citizens aged >= 18 years old; 2.Participants have clinical manifestations of chest pain and are willing to undergo examinations including coronary angiography, QCA (Quantitative Coronary Angiography), and high-frequency QRS detection; 3.Participants (or their legal guardians) are fully informed and have signed the informed consent form; 4.Participants are willing to complete the follow-up.

Exclusion criteria

Exclusion criteria: 1.General Exclusion Criteria: Participants will be excluded from enrollment if they meet any of the following criteria. (1)With malignant tumor or other diseases where the expected life expectancy is <= 1 year; (2)With moderate or severe depression or other mental illnesses; (3)History of stroke, epilepsy, or severe cognitive impairment that prevents accurate description of one’s own conditions; (4)Participants deemed by investigators unable to complete the study or unsuitable for participating in the trial. 2. Exclusion Criteria for Resting High-Frequency QRS Electrocardiogram Situations where high-frequency QRS signals cannot be collected, including but not limited to patients’ unwillingness or inability to cooperate, poor electrode contact, or inadequate signal transmission. 3. Exclusion Criteria for Exercise Stress High-Frequency QRS Electrocardiogram: Participants will be excluded from undergoing exercise stress high-frequency QRS electrocardiogram if they meet any of the following criteria, but may still be considered for resting high-frequency QRS electrocardiogram collection. (1)Acute ST-segment elevation myocardial infarction (STEMI), or non-ST-segment elevation acute coronary syndrome (NSTE-ACS) assessed as high-risk or higher; (2)Other high-risk chest pain conditions, including recurrent or progressive angina pectoris, dyspnea caused by heart failure, hemodynamic instability, gradually elevated cardiac markers, or malignant arrhythmia; (3)Situations that prevent tolerance of or interfere with the treadmill stress test for high-frequency QRS electrocardiogram, including but not limited to bradyarrhythmia, tachyarrhythmia, or motor system abnormalities; (4)Ejection fraction (EF) <= 40%, or diagnosis of acute heart failure or acute exacerbation of chronic heart failure; (5)With moderate or severe valvular heart disease, or any type of cardiomyopathy; (6)Users of cardiac pacemakers or implantable cardioverter-defibrillators (ICDs); (7)Pericardial diseases and any type of myocarditis; (8)Other situations where investigators consider exercise stress high-frequency QRS electrocardiogram to be inappropriate or unfeasible.

Design outcomes

Primary

MeasureTime frame
Coronary Angiography Results;Quantitative Flow Ratio Results;All-Cause Mortality;Recurrent myocardial infarction;Unplanned readmission for heart failure;Left ventricular ejection fraction;

Secondary

MeasureTime frame
Cardiac death;Unplanned readmission for cardiovascular disease;Unplanned Cardiovascular Surgery;

Countries

China

Contacts

Public ContactPan Hongwei

Hunan Provincial People's Hospital (The First Affiliated Hospital of Hunan Normal University)

474282550@qq.com+86 134 8731 1869

Outcome results

None listed

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