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A multicenter prospective cohort study on the diagnosis and treatment of coronary heart disease

A multicenter prospective cohort study on the diagnosis and treatment of coronary heart disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124048
Enrollment
Unknown
Registered
2026-05-06
Start date
2026-05-07
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Coronary heart disease

Interventions

Observation group:none

Sponsors

The Second Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18 - 90 years old; 2. This study refers to the "2024 ESC Guidelines for the Management of Chronic Coronary Syndrome" [19] and the "Global Definition of Myocardial Infarction" (2018) [20]. The diagnosis of coronary heart disease must meet the following criteria: any one of the following: (1). CTCA/ICA shows lumen stenosis >= 50%;(2). Previous MI or revascularization (PCI/CABG); (3). Typical angina symptoms + ischemic evidence: 1). Clinical manifestations Mainly manifested as exertional angina, with the following characteristics: Location of chest pain: behind the sternum or in the precordial area, which may radiate to the left shoulder and the inner side of the left arm;Nature of pain: a sense of oppression, tightness, or suffocation, lasting for several minutes to over ten minutes;Inducing factors: physical activity, emotional excitement, overeating, cold, etc;Relief methods: can be rapidly relieved by rest or sublingual administration of nitroglycerin. 2). Ischemic evidence (satisfying any one of the following) Electrocardiogram: resting electrocardiogram may be normal, but during angina attack, ST segment depression or T wave inversion may be observed. Echocardiography through the chest: Segmental abnormality of ventricular wall motion;Stress echocardiography: Abnormal local systolic thickening of the ventricular wall during stress;Computed tomography perfusion imaging: Manifested as low-density areas on the images. 3. There is no gender restriction for the subjects; 4. Voluntary participation in this study and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Vulnerable groups, including those with mental illness, cognitive impairment, critically ill patients, women in pregnancy, lactation or with positive pregnancy test, and those with communication and comprehension difficulties that prevent them from completing follow-up visits, etc; 2. Congenital heart disease, cardiomyopathy; 3. Patients with a history of moderate or severe valvular disease; 4. Patients with malignant tumors and an expected survival of less than 2 years; 5. History of drug or alcohol abuse within the last 12 months; 6. Hemodynamic instability requiring mechanical assistance such as IABP or ECMO.

Design outcomes

Primary

MeasureTime frame
The first MACE (A composite event of Cardiovascular death, non-fatal MI, non-fatal stroke);

Secondary

MeasureTime frame
Medication intake situation;Auxiliary examination;Symptoms and signs;Blood biochemistry, blood routine, coagulation factors, inflammatory factors, myocardial injury markers, BNP/NT-proBNP, urine routine;General demographic data;Medical history, comorbidities;

Countries

China

Contacts

Public ContactWei Wang

The Second Affiliated Hospital of the Army Medical University

weiericwang@163.com+86 23 68765491

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026