Status: Recruiting
Feasibility and Efficacy Study of the CardioPulmonary Management (CPM) System in Patients With Chronic Heart Failure
The primary purpose for this study is to support the hypothesis (pilot data) that the use of the Sensinel CPM system reduces the rate of HF-related events and the related healthcare cost. The study will also measure the impact on quality of care and patient satisfaction. In order to support the primary objective, the study will compare the outcomes and costs for patients using the Sensinel CPM system against those who are not. This can either be done using institutions' averages, if available, or through a control group.
Participants needed: 1,200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Analog Device, Inc.Updated: Aug 19, 2026Locations: 7
Eligibility criteria
NYHA Class III HF [+5]
Under 18 years of age [+10]