Trials / Recruiting
RecruitingNCT06561932
A Feasibility Study Implant of the WiSE® CRT System With an Intracardiac Pacemaker to Achieve Totally Leadless CRT
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- Sponsor
- EBR Systems, Inc. · Industry
- Sex
- All
- Age
- 22 Years
- Healthy volunteers
- Not accepted
Summary
Assess the safety and efficacy of the co-implantation of the WiSE CRT System with an intracardiac pacemaker to provide totally leadless CRT.
Detailed description
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. Single-arm, prospective, multicenter, observational study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | WiSE CRT 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. |
Timeline
- Start date
- 2025-12-18
- Primary completion
- 2027-04-01
- Completion
- 2027-04-01
- First posted
- 2024-08-20
- Last updated
- 2026-02-06
Locations
4 sites across 1 country: Australia
Source: ClinicalTrials.gov record NCT06561932. Inclusion in this directory is not an endorsement.