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Cardiomyopathy / ICD/CRT-D equipped with HeartLogic, Sleep Incline, and Apnea Scan functions / Heart Failure · Observational Study
ClinicalTrials.gov · August 7, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a planned prospective observational registry evaluating associations between device-based sensor parameters (HeartLogic, Sleep Incline, Apnea Scan) and heart failure worsening events over 15 months in patients with implanted ICDs or CRT-Ds. No results have been reported in this registry record; the study remains active and recruiting data.
Observational. Heart Failure, Cardiomyopathy; age from 19 Years. Intervention: Heart Failure or Cardiomyopathy Patients with ICD/CRT-D. n = 500. 1 site: South Korea.
This is a planned prospective observational registry evaluating associations between device-based sensor parameters (HeartLogic, Sleep Incline, Apnea Scan) and heart failure worsening events over 15 months in patients with implanted ICDs or CRT-Ds. No results have been reported in this registry record; the study remains active and recruiting data.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
Once results are published, this registry may establish whether remote device-based sensor monitoring can reliably identify heart failure worsening and support clinical decision-making. Clinicians should await published outcomes before incorporating these sensor parameters into practice.
This is an active observational registry study with no reported results; it is designed to evaluate associations between device sensors and heart failure worsening but outcome data are not yet published.
As stated by the source record.
Quoted from the source exactly as published.
Once results are published, this registry may establish whether remote device-based sensor monitoring can reliably identify heart failure worsening and support clinical decision-making. Clinicians should await published outcomes before incorporating these sensor parameters into practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07753135). This is a study registration, not published results. Lead sponsor: Samsung Medical Center. Recruitment status: ACTIVE_NOT_RECRUITING. Study type: OBSERVATIONAL. Enrollment: 500 participants (ACTUAL). Conditions: Heart Failure, Cardiomyopathy. Interventions: DEVICE: ICD/CRT-D equipped with HeartLogic, Sleep Incline, and Apnea Scan functions. Primary outcome measures: Change in Device-Based Sensor Parameters Associated With Heart Failure Worsening Events , From enrollment through the 15-month follow-up period. 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.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.