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Clinical Trials in Italy / NCT07281859
Recruiting Observational

heaRtInsiGHT Alert guIDE: RightAIDE Application of the HeartInsight Acute Heart Failure Predictor in Routine Clinical Practice: Organizational Models and Workflow.

NCT07281859 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2025-06-20
Last updated
2025-12-15

Condition(s) studied

Heart Failure

Study summary

The RightAIDE study is a prospective, multicenter, observational registry designed to evaluate the real-world application of the HeartInsight™ algorithm for predicting acute heart failure (HF) events in patients implanted with a Biotronik ICD or CRT-D device with atrial sensing and Home Monitoring capability. Heart failure is a growing public health issue with high morbidity, mortality, and healthcare costs. HeartInsight, derived and validated in the SELENE HF study, integrates temporal trends of seven physiological variables monitored by the implanted device to provide early warnings of impending acute decompensation, with a median lead time of 42 days. This study aims to collect data on the implementation of a standardized workflow for interpreting and responding to HeartInsight alerts in routine clinical practice. Approximately 100 patients across 14 centers in Italy will be enrolled and followed for 12 months. The primary endpoint is the proportion of HeartInsight alerts considered "actionable," meaning they trigger at least one predefined clinical action (e.g., device reprogramming, therapy optimization, unscheduled visits, or hospital admission). Secondary endpoints include alert frequency, cumulative alert duration, number of patient interviews performed, hospitalizations during and outside alert periods, and the proportion of patients successfully using the HeartInsight Patient App. Data will be collected via electronic case report forms (eCRFs), analyzed descriptively, and monitored for quality. The study will generate insights into integrating HeartInsight-based predictive monitoring into clinical workflows to potentially improve patient management and outcomes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * The patient has already received a de novo ICD (DR or DX) or CRT-D within no more than one year, according to guidelines, equipped with atrial sensing and a Home Monitoring system. * Documentation of heart failure of ischemic or non-ischemic origin. * At the time of device implantation: ejection fraction ≤35% and NYHA Class II or III. * Sinus rhythm. * Age ≥18 years. * The patient has signed the informed consent for participation. Exclusion Criteria: * Patients who have received the implantable device as a replacement or upgrade of a previous one. * Patients who have received the device more than one year ago. * At the time of enrollment: patient with HeartInsight previously activated. * Permanent or long-standing atrial fibrillation. * Sinus node disease with indication for atrial pacing. * At the time of enrollment: NYHA Class IV. * Planned cardiac surgery within three months following enrollment. * Life expectancy of less than one year. * Unstable residence or insufficient GSM coverage at the patient's home. * Pregnancy or breastfeeding.

Primary outcome measure(s)

Trial sites (13)

FacilityCityRegionStatus
Clinica Montevergine Mercogliano Avellino Not Yet Recruiting
Spedali Civili di Brescia Brescia Brescia Not Yet Recruiting
Presidio Ospedaliero di Rho - ASST Rhodense Rho Milano Recruiting
Ospedale San Gerardo Monza Monza Not Yet Recruiting
Ospedale Monaldi Naples Napoli Not Yet Recruiting
Ospedale Monaldi Naples Napoli Not Yet Recruiting
Ospedale Giovanni Paolo II Ragusa Ragusa Recruiting
Maria Cecilia Hospital Cotignola Ravenna Recruiting
Ospedale Civile SS. Annunziata Sassari Sassari Recruiting
Ospedale di Cattinara Trieste Trieste Not Yet Recruiting
Ospedale Mater Salutis di Legnagno Legnago Verona Recruiting
Ospedale Fracastoro San Bonifacio Verona Recruiting
Ospedale Magalini di Villafranca Villafranca di Verona Verona Recruiting

More University of Padova trials in Italy

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07281859 on ClinicalTrials.gov ↗ ← All trials in Italy