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RECRUITING
NCT07098858

The WiSE®-UP Study (The WiSE System Utilization & Performance Study)

Sponsor: EBR Systems, Inc.

View on ClinicalTrials.gov

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

Key Details

Gender

All

Age Range

22 Years - Any

Study Type

OBSERVATIONAL

Enrollment

320

Start Date

2025-11-03

Completion Date

2032-09-30

Last Updated

2026-09-10

Healthy Volunteers

No

Conditions

Interventions

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 biventricular (BiV) pacing.

Locations (12)

CardioVascular Associates of Mesa (CVAM)

Mesa, Arizona, United States

Honor Health

Scottsdale, Arizona, United States

Arrhythmia Research Group (St. Bernards Hospital)

Jonesboro, Arkansas, United States

Naples Community Hospital

Naples, Florida, United States

University of Michigan

Ann Arbor, Michigan, United States

St. Luke's Hospital of Kansas City

Kansas City, Missouri, United States

Weill Cornell Medicine

New York, New York, United States

Cleveland Clinic Foundation

Cleveland, Ohio, United States

Penn State Health

Hershey, Pennsylvania, United States

MUSC

Charleston, South Carolina, United States

Texas Cardiac Arrhythmia Research Foundation

Austin, Texas, United States

UVA

Charlottesville, Virginia, United States