Actively Recruiting

Age: 18Years +
All Genders
ID07620119

Development of a Machine Learning Model for Diagnosing Occlusive Myocardial Infarction in Patients with Left Bundle Branch Block

Led by Konya City Hospital · Updated on 2026-06-02

50

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a new method to diagnose severe heart attacks in patients who have a specific heart electrical pattern called Left Bundle Branch Block (LBBB). Diagnosing heart attacks in these patients is challenging because LBBB changes the heart's electrical signals on an ECG, hiding typical signs of blocked arteries. This observational study aims to develop and test a machine learning model that analyzes digital 12-lead ECG signals to detect true artery blockages in patients with LBBB. The study uses standard digital 12-lead ECG data collected during emergency visits and applies a machine learning model to analyze these signals for subtle patterns. The model's predictions will be compared with results from invasive coronary angiography, the gold standard for visualizing blocked vessels. The study also evaluates whether the model can distinguish between heart attacks caused by blocked arteries (Type 1 MI) and other conditions with elevated heart enzymes (Type 2 MI). Participants will have their ECG recorded when they arrive at the emergency department with chest pain or related symptoms. Researchers will compare the machine learning model's results with coronary angiography performed during the hospital stay. The main outcome measures include the accuracy of diagnosing occlusive heart attacks within about 24 hours and the ability to differentiate heart attack types during the hospital stay. Researchers will also assess whether using this tool can reduce unnecessary invasive procedures. Participation involves data collection during routine care and follow-up during the hospital stay, with the study ending after these assessments.

CONDITIONS

Brief Title

Machine Learning for Diagnosis of Occlusive MI in LBBB Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years and older presenting to the emergency department
  • Patients with acute ischemic chest pain or similar symptoms such as sudden shortness of breath, unexplained sweating, or fainting
  • Patients with confirmed Left Bundle Branch Block (LBBB) on initial 12-lead ECG, either new or chronic
  • Patients who undergo invasive coronary angiography during their hospital admission
  • Patients or their legal representatives who provide written informed consent
Not Eligible

You will not qualify if you...

  • Patients under 18 years old
  • Pregnant or breastfeeding women
  • Patients with poor-quality or unreadable digital ECG recordings due to artifacts or technical errors
  • Patients who have cardiopulmonary arrest before the initial ECG in the emergency department
  • Patients transferred from another facility who already had coronary angiography or artery treatment
  • Patients who decline or refuse to provide written informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Within 24 hours of emergency department presentation

Participants receive a standard 12-lead digital electrocardiogram (ECG) and undergo invasive coronary angiography as part of routine clinical care to diagnose occlusive myocardial infarction.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 7 days

Participants are observed during their hospital stay to assess differentiation between types of myocardial infarction and other outcomes.

Ongoing hospital stay assessments

Trial Site Locations

Total: 1 location

1

Konya City Hospital

Konya, Karatay, Turkey (Türkiye), 42100

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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