U.S., May 1 -- ClinicalTrials.gov registry received information related to the study (NCT06393842) titled 'Correlation of Non-invasive CPM Wearable Device With Measures of Congestion in Heart Failure in Exercise' on Feb. 19.
Brief Summary: 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.
Study Type: Observational
Condition: Heart Failure
Intervention: 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.
Recruitment Status: Recruiti...