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Correlation of the Non-invasive Cardiopulmonary Management (CPM) Wearable Device With Measures of Congestion in Heart Failure

NCT05026034 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 72

Last updated 2023-04-03

No results posted yet for this study

Summary

Fluid status and congestion can be determined by the CPM wearable device and correlates with invasive measures, non-invasive measures and biochemical markers of congestion and changes in congestion.

Conditions

Interventions

DEVICE

non-invasive Cardiopulmonary Management (CPM) wearable device

non-invasive Cardiopulmonary Management (CPM) wearable device with measures of congestion in heart failure

Sponsors & Collaborators

  • University of Glasgow

    collaborator OTHER

  • NHS Greater Glasgow and Clyde

    lead OTHER

Principal Investigators

  • Pardeep Jhund · Glasgow University and NHS Greater Glasgow and Clyde

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-23
Primary Completion
2022-07-22
Completion
2022-07-22

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

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 NCT05026034 on ClinicalTrials.gov