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Clinical Trials/NCT07128667
NCT07128667Not yet recruitingNot Applicable

A Prospective Cohort Study on Clinical Characteristics, Risk Factors, and Long-Term Outcomes in Young Patients With Acute Myocardial Infarction

China-Japan Friendship Hospital0 sites200 target enrollmentStarted: September 1, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
200
Primary Endpoint
Malignant arrhythmia events

Study Overview

Brief Summary

The incidence of acute myocardial infarction (AMI) in young patients is on the rise, placing a heavy health and economic burden on individuals, families, and society. The clinical phenotype and pathophysiological mechanisms of AMI in this population exhibit significant heterogeneity compared to elderly patients, and existing risk assessment tools have limited applicability in this specific group. The core problem this study aims to address is: how to accurately identify specific risk factors in young AMI patients and build an effective risk prediction model to prevent and optimize clinical diagnosis and treatment.

This study will adopt a prospective cohort design to collect multi-dimensional clinical data from young AMI patients. It will systematically analyze their clinical characteristics, risk factors, and coronary lesion status to comprehensively map the clinical, risk factor, and pathophysiological diversity of young AMI patients. Secondly, it will delve into identifying specific risk factors that influence the onset, progression, and long-term prognosis of young AMI. Thirdly, it will combine machine learning algorithms to develop a risk prediction model for young AMI, performing internal validation in the prospective cohort and external validation in the MIMIC-IV database. Simultaneously, it will explore novel biomarkers associated with disease onset and progression. The key outcomes of this study are to establish a high-quality clinical database of young AMI patients, design a risk prediction model for young AMI based on the study results, and produce high-level academic publications.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age between 18 and 45 years (inclusive of 18 and 45 years);
  • •Meeting the diagnostic criteria for acute myocardial infarction (including both ST-elevation myocardial infarction and non-ST-elevation myocardial infarction);
  • •Presenting for medical attention within 24 hours of symptom onset;
  • •The subject (or their legal representative) is willing and able to sign the informed consent form (for the prospective follow-up portion);
  • •Life expectancy greater than 1 year.

Exclusion Criteria

  • •(1) History of prior old myocardial infarction, severe valvular heart disease, or heart failure; (2) Pregnancy or lactation; (3) Mental disorders or other conditions that prevent cooperation with treatment; (4) Concomitant severe infection, inflammatory or immunological biomarker changes unrelated to AMI, trauma, or recent major surgery.

Outcomes

Primary Outcomes

Malignant arrhythmia events

Time Frame: Short-term endpoints (in-hospital and within 30 days post-discharge).Long-term endpoints (12 months post-discharge).

All-cause mortality

Time Frame: Short-term endpoints (in-hospital and within 30 days post-discharge).Long-term endpoints (12 months post-discharge).

Non-fatal myocardial infarction

Time Frame: Short-term endpoints (in-hospital and within 30 days post-discharge).Long-term endpoints (12 months post-discharge).

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
China-Japan Friendship Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Zhengqin Zhai

Dr.

China-Japan Friendship Hospital

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