Clinical Data Collection Study Using CPM System

Description

This study will assess the deployment of the ADI CPM System in a home setting and determine the interoperability of the CPM System within existing care pathways for HF patients. Clinicians will be blinded to CPM generated data and acquired physiologic data will not be used in clinical decision-making. After conclusion of this phase, a retrospective review of CPM System-acquired data will be compared with changes in treatment and HF events. This retrospective review will inform the subsequent design of the interventional study that is planned. Study participation for each patient will last for six months inclusive of 5 months of daily CPM monitoring followed by 30 days of observation for HF-related events. The additional 30 days of medical record observation is intended to capture any events that might correspond to predictions made during the final weeks of CPM monitoring.

Conditions

Heart Failure

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Study Overview

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Study Details

Study overview

This study will assess the deployment of the ADI CPM System in a home setting and determine the interoperability of the CPM System within existing care pathways for HF patients. Clinicians will be blinded to CPM generated data and acquired physiologic data will not be used in clinical decision-making. After conclusion of this phase, a retrospective review of CPM System-acquired data will be compared with changes in treatment and HF events. This retrospective review will inform the subsequent design of the interventional study that is planned. Study participation for each patient will last for six months inclusive of 5 months of daily CPM monitoring followed by 30 days of observation for HF-related events. The additional 30 days of medical record observation is intended to capture any events that might correspond to predictions made during the final weeks of CPM monitoring.

Clinical Data Collection Study Using CardioPulmonary Management System in Patients With Chronic Heart Failure

Clinical Data Collection Study Using CPM System

Condition
Heart Failure
Intervention / Treatment

-

Contacts and Locations

New York

Columbia University Medical Center, New York, New York, United States, 10032

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * NYHA Class III-IV
  • * NYHA Class II HF with one or more of the following:
  • * Chronic Kidney Disease (eGFR\<60)
  • * HF hospitalization (defined as HF listed as the major reason for hospitalization) within 9 months prior to screening visit and NT-proBNP \> 200 pg/ml for patients not in AF or \> 600 pg/m for patients in AF on screening ECG
  • * NT-proBNP \> 300 pg/ml for patients not in AF or \> 900 pg/ml for patients in AF on the screening visit ECG.
  • * Chronic obstructive pulmonary disease (COPD)
  • * Under 18 years of age
  • * Patients with severe COPD (GOLD stage III or IV)
  • * Chronic Kidney Disease (eGFR \< 20)
  • * Limited mobility preventing application of device
  • * Cognitive impairments that would limit the application and proper use of the device
  • * Skin allergies or skin sensitivities to silicone-based adhesives
  • * Pregnancy
  • * Skin breakdown on the left chest or breast area
  • * Not willing to shave chest hair if needed to apply device
  • * Patients on chronic inotropic therapy
  • * Patients with any condition that might limit the survival to less than 1 year as assessed by the investigator
  • * No cellular coverage (Patient's Home)

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Analog Device, Inc.,

Study Record Dates

2025-12-01