Overview
Observe to understand product performance, including patient safety, clinical outcomes, and CRT response information associated with the use of the market-released WiSE System
Description
The WiSE-UP Registry is a prospective, real-world, observational study aimed at understanding acute and long-term product performance, including patient safety, clinical outcomes, and CRT response information associated with the use of the market-released WiSE System.
Eligibility
- Patient or legally authorized representative can provide written authorization and/or consent per institution requirements.
- Patient is intended to receive a WiSE System and passed the acoustic window screening
- Patient who is, or will be, accessible for follow-up.
- Participation is not excluded by local law.
- Patient is not enrolled in a concurrent drug and/or device study that may confound the Registry results.
- Patient life expectancy \>1 year.