Remote Alert Pathway To Optimize CaRe of Cardiac Implantable Electrical Devices

Recruiting N/A Interventional Study
Pacemaker DDD Implantable Defibrillator User
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Beth Israel Deaconess Medical Center · Other
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About This Trial
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 Feasi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Adult aged \> 18 years 2. Clinically stable by investigator assessment 3. Has a newly implanted or existing wireless CIED: single, dual-chamber, biventricular, subcutaneous/extravascular, and leadless systems are all eligible, including pacemakers or implantable cardioverter-…
Contacts

Linda Valsdottir, MS

6176678800

lvalsdot@bidmc.harvard.edu

CONTACT