Association of Heart Failure Aggravation and Device-based Sensor Parameters
NCT: NCT07753135 · ACTIVE_NOT_RECRUITING
Brief Summary
This is a prospective, multicenter, observational patient registry designed to evaluate the association between changes in device-based sensor parameters and heart failure (HF) aggravation in patients implanted with Boston Scientific implantable cardioverter-defibrillators (ICDs) or cardiac resynchronization therapy defibrillators (CRT-Ds) equipped with HeartLogic™, Sleep Incline, and Apnea Scan functions. The study will prospectively collect remote monitoring and clinical follow-up data to determine whether changes in individual or combined device-based sensor parameters are associated with worsening HF events and to evaluate the clinical utility of remote monitoring for HF management.
Frequently Asked Questions
What is Association of Heart Failure Aggravation and Device-based Sensor Parameters?
Association of Heart Failure Aggravation and Device-based Sensor Parameters is a clinical trial registered under NCT07753135. Current status: ACTIVE_NOT_RECRUITING.
What is the status of NCT07753135?
The current status of NCT07753135 (Association of Heart Failure Aggravation and Device-based Sensor Parameters) is: ACTIVE_NOT_RECRUITING.
When did Association of Heart Failure Aggravation and Device-based Sensor Parameters start?
Association of Heart Failure Aggravation and Device-based Sensor Parameters started on 2023-02-01.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.