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Implantable Sensor in Aortic Stenosis

NCT06826183 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 17

Last updated 2025-02-13

No results posted yet for this study

Summary

To establish the relationship between a panel of biological markers obtained from the REVEAL Linq device and exercise performance as judged by cardiopulmonary exercise testing

Conditions

  • Aortic Stenosis

Interventions

DEVICE

REVEAL Linq device

Implantable loop recorder

Sponsors & Collaborators

  • East Sussex Hospitals NHS Trust

    collaborator OTHER

  • Barts & The London NHS Trust

    lead OTHER

Principal Investigators

  • Guy Lloyd · Barts & The London NHS Trust

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-15
Primary Completion
2019-03-09
Completion
2020-03-09
FDA Device
Yes

Countries

  • United Kingdom

Study Locations

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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 NCT06826183 on ClinicalTrials.gov