AVEIR DR Coverage With Evidence Development (CED) Study
Recruiting now
Conditions studied: Cardiac Pacemaker, Arrythmia, Bradycardia
In brief
The purpose of this coverage with evidence development (CED) study is to evaluate complications and long-term health outcomes of the dual chamber Aveir Leadless Pacemaker device (aka Aveir™ DR LP system).
Key facts
- Study ID
- NCT05932602
- Run by
- Abbott Medical Devices
- People needed
- 2812
- Starts
- 2023-10-31
- Expected to finish
- 2030-05-01
- Last updated by the study team
- 2025-04-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Medicare beneficiaries implanted with an Aveir DR leadless pacemaker on or after the study start date (i.e., the date of Aveir DR market approval) will be included in the study.
- OR
- Medicare beneficiaries implanted with a full system (e.g. lead and generator) dual-chamber transvenous pacemaker on or after the study start date
You may not qualify if…
- None
Where it is running
- Abbott — Sylmar, California, United States (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.