Clinical Trial

Remote Alert Pathway To Optimize CaRe of Cardiac Implantable Electrical Devices

Study acronym: RAPTOR-CIED
Recruiting
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Record status
This record was last updated January 7, 2026 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-04-18.
Status change: Not Yet Recruiting → Recruiting 2026-01-05
Trial Details
NCT Number NCT06937658
Lead Sponsor Beth Israel Deaconess Medical Center
Collaborators: Patient-Centered Outcomes Research Institute
Conditions Pacemaker DDD, Implantable Defibrillator User
Enrollment 120 participants
Start Date 2025-05-01
Primary Completion 2026-06-30 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-01-07