Clinical Data Collection Study Using CPM System
NCT: NCT06007079 · TERMINATED
Brief Summary
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.
Frequently Asked Questions
What is Clinical Data Collection Study Using CPM System?
Clinical Data Collection Study Using CPM System is a clinical trial registered under NCT06007079. Current status: TERMINATED.
What is the status of NCT06007079?
The current status of NCT06007079 (Clinical Data Collection Study Using CPM System) is: TERMINATED.
When did Clinical Data Collection Study Using CPM System start?
Clinical Data Collection Study Using CPM System started on 2023-12-06.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.