Aveir VR Real-World Evidence Post-Approval Study

Running, not enrolling

Conditions studied: Cardiac Pacemaker, Arrythmia, Bradycardia

In brief

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.

Key facts

Study ID

NCT05270499

Run by

Abbott Medical Devices

People needed

3427

Starts

2022-06-21

Expected to finish

2034-09-30

Last updated by the study team

2026-05-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Abbott — Sylmar, California, United States

Full record on ClinicalTrials.gov

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