Enhanced Prediction Model for Major Adverse Events Following Acute Myocardial Infarction

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years old

Presented with myocardial infarction, including NSTEMI and STEMI

Undergoing successful percutaneous coronary intervention.

Disqualifiers

Subjects who decline protocol-mandated follow-up or withhold informed consent.

Individuals whose expected survival is < 1 year.

Trial population

Patients with myocardial infarction

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Percutaneous coronary intervention

    Procedure/Surgery

    Percutaneous coronary intervention

Treatment groups

1,544 Participants
are divided into 1 treatment group
Group A: MI group1 intervention

Trial outcomes

Primary outcomes

1

Recurrent myocardial infarction or cardiac death

Patients received recurrent myocardial infarction or cardiac death

Time frame
At 24-month Follow-up
2

Diagnostic performance

Diagnostic performance of the AI-driven multimodal predictive model: area under the receiver-operating characteristic curve (AUC), sensitivity, specificity, overall accuracy, positive predictive value (PPV), and negative predictive value (NPV).

Time frame
At 24-month follow-up
3

MACE at 24 months

Major adverse cardiovascular events, defined as a compisite of cardiac death, myocardial infarction, target vessel revascularization.

Time frame
At 24-month follow-up

Secondary outcomes

1

MACE at 60 months

Major adverse cardiovascular events, defined as a compisite of cardiac death, myocardial infarction, target vessel revascularization.

Time frame
At 60-month follow-up

Other outcomes

1

MACE according to pre-specified subgroups

MACE stratified by sex, diabetes status, and chronic kidney disease (CKD) status.

Time frame
At 24- and 60-month follow-up
2

MACE according to physiological status

MACE prediction integrating physiological metrics-angiographic FFR, IMR, MRR, and CFR-of the culprit and non-culprit coronary arteries.

Time frame
At 24- and 60-month follow-up

Sponsors and contacts

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