NCT07352657

Remote Alert Pathway To Optimize CaRe of Cardiac Implantable Electrical Devices: The RAPTOR-CIED Study (Main Phase)

• Status: Not Yet Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 3,000 (estimated)
• Sponsor: Beth Israel Deaconess Medical Center · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

he Remote Alert Pathway to Optimize Care of Cardiac Implantable Electrical Devices (RAPTOR-CIED) Study is a pragmatic, multi-center, randomized trial with 1:1 patient-level randomization comparing the safety and effectiveness of alert-driven care versus guideline-based care for patients with wireless cardiac implantable electrical devices (CIEDs). The study will be conducted in 2 phases: a Feasibility Phase and a Main Phase. This registration outlines the goals and design features of the Main Phase of the study.

Conditions

• Pacemaker
• Implantable Defibrillator

Interventions

Type	Name	Description
OTHER	Alert-based care	Alert-based care is an alternative strategy for longitudinal management of patients with wireless pacemakers and implantable defibrillators
OTHER	Guideline-based Care	Remote monitoring programming scheduled for alert transmissions, patient-initiated transmissions, and routine transmissions (scheduled to occur every 90 days from the date of enrollment in the study); in-office interrogations on at least an annual basis

Timeline

• Start date: 2026-12-01
• Primary completion: 2030-12-31
• Completion: 2031-01-31
• First posted: 2026-01-20
• Last updated: 2026-02-06

Locations

1 site across 1 country: United States