Condition: Leadless Pacemaker · Bradycardia · AV Block · Sponsor: Biotronik, Inc.
The objective of this Investigational Device Exemption trial is to confirm the safety and performance of the LivIQ leadless pacemaker system, in patients with a Class I or II indication for ventricular pacing (VVI/VDD) according to applicable guidelines. An integrated atrioventricular synchrony sub-study (AVS) is specifically designed to evaluate the AVS performance of the LivIQ system.
This description comes directly from the study's public registry record.
Jennifer Alkire Project Manager · 800-547-0394 · US-BIO-LivIQ@biotronik.com
Andreas Peth Clinical Project Manager · +49 30 68905 1288 · BIO-LivIQ@biotronik.com
Always discuss trial participation with your own doctor first.
| Trinity Health Ann Arbor Hospital | Ypsilanti, Michigan, United States | Recruiting |
| NY Presbyterian Weill Cornell Medicine | New York, New York, United States | Recruiting |
| Wake Forest University Health | Winston-Salem, North Carolina, United States | Recruiting |
| Cardiology Consultants of Philadelphia | Paoli, Pennsylvania, United States | Recruiting |
| UVA Health University Medical Center | Charlottesville, Virginia, United States | Recruiting |
| Princess Alexandra Hospital | Woolloongabba, Queensland, Australia | Recruiting |
| Victorian Heart Hospital | Clayton, Victoria, Australia | Recruiting |
| AZ Sint-Jan | Bruges, Belgium | Recruiting |
| Jessa Ziekenhuis | Hasselt, Belgium | Recruiting |
| UZ Leuven Gasthuisberg | Leuven, Belgium | Recruiting |
| CHR de la Citadelle - Liège | Liège, Belgium | Recruiting |
| Hôpital Gabriel Montpied, Clermont Ferrand | Clermont-Ferrand, France | Recruiting |
+ 8 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07118358