VITARIA Registry Study
NCT02545582 · Status: SUSPENDED · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2017-01-31
Summary
This registry will observe patients with symptomatic heart failure with implantable vagus nerve stimulation to provide insights into safety and efficacy during clinical routine.
Conditions
- Congestive Heart Failure
Interventions
- DEVICE
-
VITARIA System
Implantable vagus nerve stimulator
Sponsors & Collaborators
-
Cyberonics, Inc.
lead INDUSTRY
Principal Investigators
-
Helmut Klein, MD · CRI GmbH
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-08-31
- Primary Completion
- 2018-08-31
- Completion
- 2019-12-31
Countries
- Germany
Study Locations
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