RecruitingNCT05270499
Aveir VR Real-World Evidence Post-Approval Study
Studying OBSOLETE: Sino-auricular heart block
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Abbott Medical Devices
- Principal Investigator
- Nicole HarbertAbbott
- Intervention
- Aveir VR Leadless Pacemaker System(device)
- Enrollment
- 2100 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2034
Study locations (1)
- Abbott, Sylmar, California, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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