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

NCT07098858 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 320

Last updated 2026-02-13

No results posted yet for this study

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

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.

Sponsors & Collaborators

  • EBR Systems, Inc.

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-03
Primary Completion
2032-09-30
Completion
2032-09-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07098858 on ClinicalTrials.gov