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Clinical Trials/NCT03600259
NCT03600259
Recruiting
Not Applicable

Cohort Study of Acute Myocardial Infarction in Tianjin

Tianjin Chest Hospital1 site in 1 country13,000 target enrollmentJanuary 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myocardial Infarction, Acute
Sponsor
Tianjin Chest Hospital
Enrollment
13000
Locations
1
Primary Endpoint
Cardiac death
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Acute myocardial infarction(AMI) is the most serious manifestation of coronary artery disease. AMI is characterized by high mortality, high disability, and high cost. However, multicenter research on AMI with large sample size in Tianjin or even China is limited. By including AMI in 36 hospitals,this multicenter study will capture the changes in epidemiological trends ,analyze the status of treatment in Tianjin, and explore the best treatment strategies.

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
December 1, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yin Liu,MD

Director, Cardiology Department, Tianjin Chest Hospital

Tianjin Chest Hospital

Eligibility Criteria

Inclusion Criteria

  • Hospitalized patients with acute myocardial infarction according to Cardiac biomarker values \[Selective cardiac troponin (cTc) elevation and/or decline detection, at least one value exceeds the 99% reference limit (URL) and at least one of the following:(1)Symptoms of myocardial ischemia;(2)New or suspected new obvious ST-T changes or new left bundle branch block (LBBB);(3)ECG pathological Q waves;(4)Image evidence of recent loss of viable myocardium, or new regional wall motion abnormalities;(5)Coronary thrombosis confirmed by angiography or autopsy.\]

Exclusion Criteria

  • Those who did not meet the diagnosis of acute myocardial infarction (no myocardial ischemia-related symptoms, elevation of markers of myocardial necrosis and imaging findings of myocardial infarction); those who met the inclusion criteria but refused to participate in the study; The researchers judged that the subjects had poor compliance and could not Complete follow-up as required.

Outcomes

Primary Outcomes

Cardiac death

Time Frame: 1 year

Due to recent cardiac causes (eg myocardial infarction, low-volume heart failure, fatal arrhythmias), any deaths from unknown and unexplained deaths and all surgical-related deaths (including treatment-related deaths) will be attributed to cardiac death.Unless there is a clear non-cardiological cause, all deaths are considered heart disease. Specifically, even patients with concurrent potentially fatal non-cardiac diseases (such as cancer, infections) who have any accidental death should be classified as having a heart attack.

Secondary Outcomes

  • Major adverse cardiovascular events(1 year)

Study Sites (1)

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