Perioperative Myocardial Injury in Patients Undergoing Coronary Artery Bypass Grafting: A Prospective Clinical Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-80
SponsorSecond Hospital of Jilin University

About this trial

Perioperative myocardial injury (PMI) following coronary artery bypass grafting (CABG) is associated with postoperative morbidity, mortality, and long-term outcomes. High-sensitivity troponin assays and cardiac MRI offer reliable diagnostic tools for PMI, but evidence regarding optimal diagnostic thresholds and perioperative imaging strategy is limited. This prospective clinical study aims to determine the incidence of perioperative myocardial injury using multimodal assessments including high-sensitivity troponin, electrocardiogram, echocardiography, cardiac MRI, and perioperative cardiovascular events.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 21 years

Undergoing CABG for unstable angina

Able to provide written informed consent

No major cardiovascular event in the prior 6 months

Disqualifiers

Significant hepatic, renal, or other major organ dysfunction

Pregnancy or breastfeeding

Withdrawal during the study

Contraindication to cardiac MRI (metal implants, claustrophobia, etc.)

Trial population

Adult patients diagnosed with unstable angina and scheduled to undergo isolated coronary artery bypass grafting (CABG) at the Second Hospital of Jilin University. All participants receive routine perioperative clinical evaluations. The study includes patients aged 21 years or older who provide written informed consent and have had no major cardiovascular events within the previous 6 months. Patients with severe organ dysfunction, pregnancy, or contraindications to cardiac MRI are excluded.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • High-Sensitivity Troponin

    Diagnostic test

    High-sensitivity troponin levels are measured preoperatively, predischarge, and at 6-month follow-up to assess perioperative myocardial injury.

  • Cardiac MRI

    Diagnostic test

    A diagnostic assessment panel including high-sensitivity troponin testing, electrocardiography, echocardiography, and cardiac magnetic resonance imaging performed during the perioperative period.

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: CABG Patients2 interventions

Trial outcomes

Primary outcomes

1

Incidence of Perioperative Myocardial Injury (PMI)

Perioperative myocardial injury defined by elevation of high-sensitivity troponin above the 99th percentile upper reference limit together with new myocardial injury detected by cardiac MRI or supportive ECG/echocardiographic changes. PMI is assessed using laboratory testing and imaging performed preoperatively, within 48 hours post-CABG, and at discharge.

Time frame
Within 48 hours post-CABG

Secondary outcomes

Other outcomes

Sponsors and contacts

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