Echocardiography: Value and Accuracy at REst and STress

NCT03674255 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 23000

Last updated 2026-04-29

No results posted yet for this study

Summary

EVAREST will identify and validate novel blood and imaging biomarkers of potential value for consistent and accurate interpretation of stress echocardiography. During phase one, blood samples will be collected to assess the impact of cardiac stress on levels of circulating biomarkers and examine whether the measurement of these biomarkers can provide additional prognostic information. Phases one, two and three will also determine whether novel imaging biomarkers can be identified in the echocardiograms that can be used for objective interpretation of the stress echocardiograms. EVAREST will recruit up to 8000 patients (First 500 during phase one, an additional 500 during phase two and an additional 7000 during phase three) from multiple hospitals across United Kingdom, who have been referred for a stress echocardiogram as part of their investigations into ischaemic heart disease. Phase four of the study will continue into a clinical study cohort phase to capture information from all patients referred for a stress echocardiogram in the UK, regardless of the reason for investigation.This registry phase will run for 2 years, recruiting up to 15000 participants.

Conditions

Sponsors & Collaborators

  • Oxford University Hospitals NHS Trust

    collaborator OTHER
  • Royal United Hospital Bath NHS Trust

    collaborator OTHER
  • Tameside Hospital NHS Foundation Trust

    collaborator OTHER
  • Royal Berkshire NHS Foundation Trust

    collaborator OTHER_GOV
  • East Lancashire Hospitals NHS Trust

    collaborator OTHER
  • Bradford Teaching Hospitals NHS Foundation Trust

    collaborator OTHER_GOV
  • Calderdale and Huddersfield NHS Foundation Trust

    collaborator OTHER
  • Great Western Hospitals NHS Foundation Trust

    collaborator OTHER
  • Mid Essex Hospital NHS Trust

    collaborator OTHER
  • Buckinghamshire Healthcare NHS Trust

    collaborator OTHER
  • Wrightington, Wigan and Leigh NHS Foundation Trust

    collaborator OTHER
  • Chelsea and Westminster NHS Foundation Trust

    collaborator OTHER
  • Milton Keynes University Hospital NHS Foundation Trust

    collaborator OTHER_GOV
  • University Hospitals Bristol and Weston NHS Foundation Trust

    collaborator OTHER
  • North Middlesex University Hospital

    collaborator OTHER
  • Northumbria Healthcare NHS Foundation Trust

    collaborator OTHER
  • London North West Healthcare NHS Trust

    collaborator OTHER
  • St George's University Hospitals NHS Foundation Trust

    collaborator OTHER
  • Ultromics Ltd

    collaborator INDUSTRY
  • National Institute for Health Research, United Kingdom

    collaborator OTHER_GOV
  • King's College Hospital NHS Trust

    collaborator OTHER
  • Guy's and St Thomas' NHS Foundation Trust

    collaborator OTHER
  • Poole Hospital NHS Foundation Trust

    collaborator OTHER
  • Blackpool Teaching Hospitals NHS Foundation Trust

    collaborator OTHER
  • Mid Yorkshire Teaching NHS Trust

    collaborator OTHER
  • Northampton General Hospital NHS Trust

    collaborator OTHER
  • North West Anglia NHS Foundation Trust

    collaborator UNKNOWN
  • Yeovil District Hospital NHS Foundation Trust

    collaborator OTHER
  • East Suffolk and North Essex NHS Foundation Trust

    collaborator OTHER
  • Nottingham University Hospitals NHS Trust

    collaborator OTHER
  • Hampshire Hospitals NHS Foundation Trust

    collaborator OTHER
  • Lantheus Medical Imaging

    collaborator INDUSTRY
  • University of Oxford

    lead OTHER

Principal Investigators

  • Paul Leeson · Cardiovascular Clinical Research Facility, University of Oxford

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2021-03-31
Completion
2033-09-30

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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 NCT03674255 on ClinicalTrials.gov