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Medtronic is sponsoring the Micra AV Registry using the Micra AV system for continued surveillance of chronic atrioventricular synchronous pacing as intended, through the collection of data based on routine clinical care practice, following commercial release. The Micra AV Registry is conducted within Medtronic's Product Surveillance Registry (PSR) platform.
The Micra AV Registry is a global, prospective, observational, multi-site registry. Patients enrolled in the Micra AV Registry will be prospectively followed for a minimum of 3 years post-implant or until registry closure, patient death, patient exit from the registry (i.e., withdrawal of consent). Enrolled patients will have scheduled follow-up visits at least annually or as prompted by reportable adverse events; however, all Micra AV system follow-up patient visits are to be reported. Therefore, if more frequent scheduled visits occur per a provider's routine clinical care practice, those visits are reported. The total estimated registry duration is 4.5 years
Age
All ages
Sex
ALL
Healthy Volunteers
No
The University of Alabama at Birmingham
Birmingham, Alabama, United States
Eisenhower Desert Cardiology Center
Rancho Mirage, California, United States
Sequoia Hospital
Redwood City, California, United States
Yale New Haven Health System
New Haven, Connecticut, United States
Baptist Health
Jacksonville, Florida, United States
Emory University Hospital
Atlanta, Georgia, United States
Indiana University Health Methodist Research Institute
Indianapolis, Indiana, United States
Iowa Heart Center
West Des Moines, Iowa, United States
University of Kansas Medical Center Research Institute
Kansas City, Kansas, United States
Saint Elizabeth Healthcare
Edgewood, Kentucky, United States
Start Date
February 8, 2020
Primary Completion Date
September 5, 2025
Completion Date
January 14, 2026
Last Updated
February 4, 2026
802
ACTUAL participants
Micra AV Transcatheter Pacing System
DEVICE
Lead Sponsor
Medtronic
NCT07221682
NCT03008291
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07290595