NCT06393842View on ClinicalTrials.gov

Correlation of Non-invasive CPM Wearable Device With Measures of Congestion in Heart Failure in Exercise

RecruitingOBSERVATIONAL
Enrollment

60

Participants

Timeline

Start Date

March 22, 2024

Primary Completion Date

February 6, 2025

Study Completion Date

February 6, 2026

Conditions
Heart Failure
Interventions
DEVICE

Cardiopulmonary Management Wearable Device

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

Trial Locations (1)

G12 8TA

RECRUITING

Glasgow Cardiovascular Research Centre, Glasgow

Sponsors

Collaborators (1)

Analog Devices
All Listed Sponsors
collaborator

Analog Devices

UNKNOWN

lead

NHS Greater Glasgow and Clyde

OTHER

NCT06393842 - Correlation of Non-invasive CPM Wearable Device With Measures of Congestion in Heart Failure in Exercise | Biotech Hunter | Biotech Hunter