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A multicenter prospective cohort study on the diagnosis and treatment of acute myocardial infarction

A multicenter prospective cohort study on the diagnosis and treatment of acute myocardial infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121017
Enrollment
Unknown
Registered
2026-03-24
Start date
2026-03-24
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

acute myocardial infarction

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. Meets the above diagnostic criteria for acute myocardial infarction; 2. Age 18-90 years; any gender; 3. Voluntarily participates in this study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Vulnerable groups, including individuals with mental illness, cognitive impairment, critically ill patients, women who are pregnant, breastfeeding, or have positive pregnancy tests, and those with communication or comprehension difficulties who cannot complete follow-up; 2. Patients with a history of dilated cardiomyopathy, peripartum cardiomyopathy, chemotherapy-induced cardiomyopathy, hereditary hypertrophic cardiomyopathy, infiltrative cardiomyopathy, or viral myocarditis; 3. Patients with a history of moderate or severe valvular disease; 4. Severe liver dysfunction not caused by cardiac reasons (ALT or AST exceeding 3 times the upper limit of normal (ULN), or total bilirubin >1.5 mg/dL), or renal dysfunction (eGFR <60 mL/min/1.73 m^2); 5. Patients with malignant tumors with an expected survival of less than 6 months; 6. History of drug or alcohol abuse within the past 12 months; 7. Hemodynamic instability requiring device assistance such as IABP or ECMO.

Design outcomes

Primary

MeasureTime frame
MACE (A composite event of all-cause death, recurrent angina pectoris, non-fatal myocardial infarction, severe arrhythmia, heart failure, and ischemic stroke);

Secondary

MeasureTime frame
blood coagulation factor;Symptoms and signs;auxiliary examination;BNP/NT-proBNP;Medication intake situation;coronary angiogram;Markers of myocardial injury;urine routines indicators;inflammatory factor;blood routine examination indicators;Blood biochemical indicators;

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: Sep 19, 2026