Machine Learning in Quantitative Stress Echocardiography

NCT04193475 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1250

Last updated 2026-02-17

No results posted yet for this study

Summary

Greater diagnostic accuracy is required to find out who is at risk of a heart attack as this can reduce the requirement of more invasive downstream tests and thereby improve the patient experience and also reduce their exposure to risk. Stress echocardiography is a routine clinical test that involves using ultrasound to image the heart whilst it is under stress to assess the risk of a heart attack.

This study will focus on developing more accurate analysis tools to interpret the results of these stress echocardiographic scans. New methods will be tested to measure the function of each part of the heart muscle, using advanced analysis of the information obtained when high-frequency sound waves are bounced off the heart inside the chest. The researchers will measure and report exact heart function during stress, so that they will be able to recognise normal hearts and those with any disease. New computer methods will be developed to display any abnormality, which will make it easier for doctors to choose the best treatment for patients who are at risk.

The goals and potential benefits of this research proposal are to update the interpretation of a routinely used clinical test (stress echocardiography) to produce a reliable new method for diagnosing the precise effects of diseased arteries on the function of the heart muscle; to develop new computer graphics that adapt to show individual risks for each patient; and to implement new computer models that can be constantly updated

Conditions

Interventions

OTHER

Analysis

No intervention planned. Novel analysis of echocardiographic data.

Sponsors & Collaborators

  • Barts & The London NHS Trust

    collaborator OTHER
  • Cardiff and Vale University Health Board

    collaborator OTHER_GOV
  • Hull University Teaching Hospitals NHS Trust

    lead OTHER_GOV

Eligibility

Min Age
20 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-22
Primary Completion
2021-08-01
Completion
2026-03-01

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04193475 on ClinicalTrials.gov