U.S., Aug. 2 -- ClinicalTrials.gov registry received information related to the study (NCT07098858) titled 'The WiSE(R)-UP Registry (The WiSE System Utilization & Performance Registry)' on July 10.
Brief Summary: Observe to understand product performance, including patient safety, clinical outcomes, and CRT response information associated with the use of the market-released WiSE System
Study Start Date: Sept. 01
Study Type: OBSERVATIONAL
Condition:
Heart Failure
Intervention:
DEVICE: The Wise System
The WiSE CRT System is an implantable cardiac system to provide left ventricular (LV) pacing stimulation in conjunction with a co-implanted system that provides right ventricular (RV) stimulation. In combination, the devices deliver bive...