Study on High-sensitivity Troponin 0h/1h for Rapid Diagnosis of Non-ST-segment Elevation Myocardial Infarction in the Chinese Population

Beijing Anzhen Hospital400 enrolled

Overview

The purpose of the study is to establish a high-sensitivity troponin 0h/1h process for the diagnosis of patients suspected of NSTEMI for the Chinese population, obtain the inclusion and exclusion criteria for diagnosis of these patients and compare the new process with the existing diagnosing methods and processes, including the 3h and 6h processes more extensively used at present and the ECG combined with troponin diagnosis, so as to explore a confirmation model suitable for the Chinese population.

Study Type

OBSERVATIONAL

Enrollment

400

Conditions

Non-ST-segment Elevation Myocardial Infarction

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Patients experiencing acute chest pain or angina pectoris symptom within 12 hours before visiting the hospital; 2. Or those experiencing acute chest pain or angina pectoris peak within 12 hours before visiting the hospital. Exclusion Criteria: Patients showing ST-segment elevation during ECG and pregnant women.

Locations (1)

Beijing Anzhen Hospital, Capital Medical University

Beijing, China

Outcomes

Primary Outcomes

Diagnosis of non-ST-segment elevation myocardial infarction

Time frame: After measuring the high-sensitivity troponin level at 1h or 3h

Secondary Outcomes

Cardiovascular events or death

Time frame: Follow-up for 6 months after diagnosis