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Application of timely detection of myocardial injury markers in pre-hospital first aid of NSTE-ACS patients

Application of timely detection of myocardial injury markers in pre-hospital first aid of NSTE-ACS patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107704
Enrollment
Unknown
Registered
2025-08-18
Start date
2025-08-18
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Non-ST segment elevation acute coronary syndrome

Interventions

Observation group:None

Sponsors

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. >=40 years old; 2. Acute chest pain/chest discomfort (occurring within the last 12 hours and lasting more than 15 minutes), suspected acute coronary syndrome; 3. Acute dyspnea, except for pulmonary diseases (asthma, COPD, pneumonia); 4. Any other clinically suspicious ACS patients; 5. Agree to participate in the study, and the patient or relative signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Age< 18 years old; 2. Cardiac arrest; 3. Patients referred from other hospitals; 4. Acute ST-segment elevation myocardial infarction; 5. Chest pain caused by other non-myocardial ischemic causes can be determined; 6. Chest pain symptoms that can be confirmed not caused by ACS: such as pneumothorax, acute pulmonary embolism, aortic dissection lesion, acute gastrointestinal disease, chronic obstructive pulmonary dysfunction, trauma, rheumatic diseases or cancer, etc.; 7. Initial electrocardiogram (ECG) showing ST-segment elevation or new LBBB can diagnose AMI episode without myocardial marker detection; 8. Other clinical manifestations that may lead to elevated troponin I, such as pregnancy, skeletal myopathy, or renal insufficiency; 9. Refusal to participate in the investigator.

Design outcomes

Primary

MeasureTime frame
The consistency of the first treatment site, ambulance POCT test results and emergency myocardial marker test results.;Diagnostic efficacy;

Secondary

MeasureTime frame
Transfer admission time;Time to receive treatment;Emergency/discharge time;hospitalization time;in-hospital mortality;

Countries

China

Contacts

Public ContactGuo Wei

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University

Guowei1010@126.com+86 136 2128 9067

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026