Prospective Acute Myocardial Infarction Data Bank

N/ANot Yet RecruitingNCT05121818

Shanghai Zhongshan Hospital3,000 enrolled

Overview

In order to accelerate border crossing between basic research and clinical research in acute myocardial infarction, it is necessary to easily use clinical and biological data. That is the reason why it is very important to create a clinical, biological and pathologic database of acute myocardial infarction, mainly prospective. All data are from patients treated in 5 centers in Shanghai，including Zhongshan Hospital of Fudan University, Shanghai Renji Hospital，Shanghai Tenth People's Hospital，Shanghai First People's Hospital, and Shanghai Tongji Hospital.

Study Type

OBSERVATIONAL

Enrollment

3,000

Conditions

Acute Myocardial Infarction

Interventions

PCIPROCEDURE

Primary percutaneous coronary intervention

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Acute myocardial infarction was diagnosed based on the Fourth Universal Definition of Acute myocardial infarction criteria. The term acute myocardial infarction should be used when there is acute myocardial injury with clinical evidence of acute myocardial ischaemia and with detection of a rise and/or fall of cTn values with at least one value above the 99th percentile URL and at least one of the following: Symptoms of myocardial ischaemia; New ischaemic ECG changes; Development of pathological Q waves; Imaging evidence of new loss of viable myocardium or new regional wallmotion abnormality in a pattern consistent with an ischaemic aetiology; Identification of a coronary thrombus by angiography or autopsy. Exclusion Criteria: * life expectancy of less than 12 months * malignant tumor * pregnancy or plans of pregnancy in the one year * any anticoagulation therapy such as heparin within 24 hours of baseline blood sampling

Locations (1)

Zhongshan Hospital

Shanghai, Shanghai Municipality, China

Outcomes

Primary Outcomes

Database of patients with acute myocardial infarction

Time frame: 5 years

Data from ClinicalTrials.gov

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