NCT05327101

Patient Preferences for Leadless Pacemakers

Quantifying Patient Preferences for Leadless Pacemaker Devices

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 117 (actual)
• Sponsor: Abbott Medical Devices · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: —

Summary

Prospective, non-randomized, multi-center study designed to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers

Detailed description

The purpose of this study is to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers. The preference study is designed to elicit patient preferences for risks and features that vary between a dual chamber leadless pacemaker system and a dual chamber transvenous pacemaker system, to quantify their relative importance.

Conditions

• Cardiac Rhythm Disorder
• Bradycardia
• Cardiac Pacemaker Artificial

Interventions

Type	Name	Description
OTHER	Patient Preference Survey	Patient preference survey on implantable cardiac pacemaker systems

Timeline

• Start date: 2022-03-28
• Primary completion: 2023-06-13
• Completion: 2023-06-13
• First posted: 2022-04-14
• Last updated: 2025-02-20
• Results posted: 2025-02-20

Locations

11 sites across 1 country: United States