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Prediction of Left Ventricular Adverse Remodeling and Major Adverse Cardiovascular Events in Patients With Acute ST-segment Elevation Myocardial Infarction Though Plasma Multiomics Analysis

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Age ≥18 years and ≤80 years.

• Definite diagnosis of STEMI according to ESC/ACC guidelines:

‣ 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).

• First STEMI (no prior history of myocardial infarction).

• Left ventricular ejection fraction (by echocardiography within 24-48 hours after admission) ≥35%.

• Informed consent: Signed informed consent obtained, with willingness to undergo serial blood sampling and echocardiographic follow-up.

Locations
Other Locations
China
Beijing Anzhen Hospital, Capital Medical University.
RECRUITING
Beijing
Contact Information
Primary
Xu Wang, Dr.
huaianwangxu@126.com
+8617810688257
Time Frame
Start Date: 2025-05-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 1000
Treatments
Patients with STEMI
First-STEMI patients treated with primary PCI (symptom-to-PCI ≤12 h, TIMI 3) were enrolled within 24 h post-PCI.
Related Therapeutic Areas
Sponsors
Leads: Beijing Anzhen Hospital
Collaborators: Beijing Jishuitan Hospital, Institute of Biophysics, Chinese Academy of Sciences

This content was sourced from clinicaltrials.gov