Clinical Trial TitleHis Bundle Pacing registry.
Clinical Trial Protocol Description:
The purpose of this study is to gain a broader understanding of the His Bundle Pacing (HBP) device implant and follow-up workflows, including device programming. The registry will include patients undergoing implantation of an Abbott pacemaker, defibrillator or CRT pacemaker or defibrillator according to routine care. There are 75 participating centers worldwide and Rush plans to enroll approximately 25 patients.
Clinical Trial Eligibility Criteria:
In order to participate you must meet the following criteria:
- Are at least 18 years of age.
- Are scheduled for implantation of an Abbott pacemaker, defibrillator of CRT-P/D device with a pacing lead located at the His bundle according to routine care.
You will be excluded from the study if any of the following criteria apply to you:
- Have a history of tricuspid valve repair or replacement.
- Have a history of previously failed HBP implant.
This is a partial list of inclusion and exclusion criteria.