Actively Recruiting

Age: 60Years +
All Genders
ID06580158

Clinical Utility of AI-Enabled Electrocardiograms to Diagnose Aortic Stenosis and Diastolic Dysfunction in Outpatient Practice

Led by Mayo Clinic · Updated on 2026-03-04

2000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating two newly developed artificial intelligence-enabled electrocardiogram (AI-ECG) models designed to detect aortic stenosis and diastolic dysfunction in outpatients aged 60 and older. These AI-ECG models show promising sensitivity and specificity but have not yet been tested prospectively to assess their real-world diagnostic and prognostic value, especially in settings with limited access to advanced medical care. Participants undergo their standard outpatient electrocardiogram (ECG), which is then processed through the AI-ECG Dashboard. If the AI-ECG indicates possible aortic stenosis or diastolic dysfunction, patients will receive a point-of-care ultrasound to confirm the diagnosis. The study is observational and involves no additional experimental treatments. During the study, researchers will track the number of patients with positive AI-ECG results and the quality of their ultrasound images. They will also compare AI-ECG findings with traditional transthoracic echocardiogram results. The study aims to understand the usefulness of AI-ECG in routine outpatient practice, with participation ongoing until March 2027.

CONDITIONS

Brief Title

AI in Outpatient Practice for Diagnosing Aortic Stenosis and Diastolic Dysfunction

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 60 years of age or older
  • Scheduled for a clinical electrocardiogram (ECG)
  • Able to provide consent
Not Eligible

You will not qualify if you...

  • Younger than 59 years of age
  • Not scheduled for a clinical ECG
  • Unable to provide 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 - Day of ECG and ultrasound

Participants undergo outpatient electrocardiograms processed through the AI-ECG Dashboard and a point of care ultrasound to confirm diagnosis.

1 visit (in-person)

Long-term Monitoring

Duration - Up to study completion in March 2027

Participants are observed for diagnostic outcomes comparing AI-ECG and ultrasound results.

Visit schedule as per routine outpatient care

Trial Site Locations

Total: 1 location

1

Mayo Clinic

Rochester, Minnesota, United States, 55905

Actively Recruiting

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Research Team

B

Brian Rudquist

J

Jae Oh, M.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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