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The WiSE®-UP Study (The WiSE System Utilization & Performance Study)
RecruitingObservational study
Who can join
Ages 22 and older · All sexes
Full eligibility criteria
* 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.
About the study
Observe to understand product performance, including patient safety, clinical outcomes, and CRT response information associated with the use of the market-released WiSE System
What is being tested
- The Wise System (device)
Sponsor: EBR Systems, Inc. · Participants: 320 · Started: Nov 3, 2025
Contact the study team
- Jamie Burke · Phone: 17194644185
Official record on ClinicalTrials.gov — NCT07098858
Locations in the U.S.
| Arizona | CardioVascular Associates of Mesa (CVAM), Mesa (Not yet recruiting) Honor Health, Scottsdale |
| Arkansas | Arrhythmia Research Group (St. Bernards Hospital), Jonesboro |
| Florida | Naples Community Hospital, Naples |
| Michigan | University of Michigan, Ann Arbor |
| Missouri | St. Luke's Hospital of Kansas City, Kansas City |
| New York | Weill Cornell Medicine, New York |
| Ohio | Cleveland Clinic Foundation, Cleveland |
| Pennsylvania | Penn State Health, Hershey |
| South Carolina | MUSC, Charleston |
| Texas | Texas Cardiac Arrhythmia Research Foundation, Austin |
| Virginia | UVA, Charlottesville |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.