Prediction of LVAR and MACE in STEMI Though Plasma Multiomics Analysis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorBeijing Anzhen Hospital

About this trial

To identify plasma multi-omics biomarkers that predict left ventricular adverse remodeling (LVAR) and major adverse cardiovascular events (MACE) in patients with acute ST-segment elevation myocardial infarction, and to investigate the molecular pathways linked to LVAR and MACE.

Eligibility criteria

Qualifiers

Age ≥18 years and ≤80 years.

Chest pain lasting >30 minutes, and

ST-segment elevation in at least two contiguous leads: ≥0.2 mV in leads V2-V3 (≥0.2 mV for men, ≥0.15 mV for women) or ≥0.1 mV in other leads, or new-onset left bundle branch block.

Reperfusion therapy: Symptom onset to first medical contact ≤12 hours, and successful primary PCI (culprit vessel opened, post-procedure TIMI flow grade 3).

Disqualifiers

Non-atherosclerotic MI: coronary embolism, spasm, aortic dissection, myocarditis, Takotsubo.

Prior HF (NYHA ≥II);

Severe CKD (eGFR <30 mL/min/1.73m² or dialysis);

Severe liver disease (Child-Pugh B/C);

Trial design

Treatments tested in this trial

  • Diagnostic Test: echocardiography and blood collection

Treatment groups

1,000 Participants
are divided into 1 treatment group

Sponsors and collaborators

Beijing Anzhen Hospital

Lead sponsor

Beijing Jishuitan Hospital

Collaborator

Institute of Biophysics, Chinese Academy of Sciences

Collaborator