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Clinical Trials in China / NCT07250152
Starting soon Observational

Enhanced Prediction Model for Major Adverse Events Following Acute Myocardial Infarction

NCT07250152 · tracked via the Priya Life Science China tracker
Sponsor
Second Affiliated Hospital, Zhejiang University, School of Medicine
Phase
Observational
Started
2025-12-01
Last updated
2025-11-26

Condition(s) studied

Myocardial Infarction (MI)

Investigational drug(s) / intervention(s)

Percutaneous coronary intervention

Percutaneous coronary intervention: Percutaneous coronary intervention

Study summary

Acute myocardial infarction (AMI) remains a leading cause of mortality worldwide. Although early revascularization has markedly improved short-term outcomes, the incidence of major adverse cardiovascular events after the index event remains unacceptably high, posing a formidable clinical challenge. Contemporary risk-stratification instruments rely predominantly on a restricted set of conventional clinical variables and therefore fail to capture the full spectrum of individual pathophysiological complexity. To overcome these limitations, the present investigation aims to develop a post-AMI prognostic model that integrates comprehensive multimodal data.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥18 years old 2. Presented with myocardial infarction, including NSTEMI and STEMI 3. Undergoing successful percutaneous coronary intervention. Exclusion Criteria: 1. Subjects who decline protocol-mandated follow-up or withhold informed consent. 2. Individuals whose expected survival is \< 1 year.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Second Affiliated Hospital of Zhejiang University School of Medicine Hangzhou Zhejiang

More Second Affiliated Hospital, Zhejiang University, School of Medicine trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07250152 on ClinicalTrials.gov ↗ ← All trials in China