Real-World Experience - Barostim™ Advancing the Level of Clinical Evidence (REBALANCE Registry)
NCT04502316 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 5000
Last updated 2026-05-11
Summary
The purpose of this registry is to develop valid scientific evidence of the safety and benefit of Barostim Therapy in the commercial setting in patients with heart failure with reduced ejection fraction (HFrEF) that were recently implanted with the Barostim System.
Conditions
Interventions
- DEVICE
-
Barostim™ System
Implantation of the Barostim™ System
Sponsors & Collaborators
-
CVRx, Inc.
lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-06-26
- Primary Completion
- 2028-06-30
- Completion
- 2028-06-30
- FDA Device
- Yes
Countries
- United States
Study Locations
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