NCT06937658

Remote Alert Pathway To Optimize CaRe of Cardiac Implantable Electrical Devices

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 120 (estimated)
• Sponsor: Beth Israel Deaconess Medical Center · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The 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 Feasibility Phase of the study.

Conditions

• Pacemaker DDD
• Implantable Defibrillator User

Interventions

Type	Name	Description
DEVICE	Alert-based care	Alert-based care is an alternative strategy for longitudinal management of patients with wireless pacemakers and implantable defibrillators
DEVICE	Guideline-based care	Guideline-based care is the current typical standard for longitudinal management of patients with wireless pacemakers and implantable defibrillators

Timeline

• Start date: 2025-05-01
• Primary completion: 2026-06-30
• Completion: 2026-06-30
• First posted: 2025-04-22
• Last updated: 2026-01-07

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study