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RECRUITING

NCT05270499

Aveir VR Real-World Evidence Post-Approval Study

Sponsor: Abbott Medical Devices

View on ClinicalTrials.gov

Summary

The purpose of this post-approval study is to evaluate the long-term safety of the single-chamber Aveir VR leadless pacemaker using real-world evidence methods.

Official title: Aveir Single-Chamber Leadless Pacemaker Real-World Evidence Post-Approval Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

2100

Start Date

2022-06-21

Completion Date

2034-02-28

Last Updated

2024-08-20

Healthy Volunteers

Conditions

Cardiac Pacemaker Arrythmia Bradycardia

Interventions

DEVICE

Aveir VR Leadless Pacemaker System

This study will utilize real-world data from patients implanted with the Aveir VR Leadless Pacemaker System. No device intervention will be conducted in this study.

Locations (1)

Abbott

Sylmar, California, United States