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RECRUITING

NCT05935007

Aveir DR 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 dual-chamber Aveir DR leadless pacemaker using real-world evidence methods.

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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

1805

Start Date

2023-10-31

Completion Date

2030-01

Last Updated

2025-04-04

Healthy Volunteers

Conditions

Cardiac Pacemaker Arrythmia Bradycardia

Interventions

DEVICE

Aveir DR Leadless Pacemaker System

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

Locations (1)

Abbott

Sylmar, California, United States