Algovita Post-Market Clinical Study: Spinal Cord Stimulation to Treat Chronic Pain
NCT02373540 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 91
Last updated 2020-08-21
Summary
The purpose of this study is to obtain real-world clinical outcome data for the Algovita Spinal Cord Stimulation system when used, on-label, according to the applicable directions for use.
Conditions
Interventions
- DEVICE
-
Algovita Spinal Cord Stimulation system
Sponsors & Collaborators
-
Bright Research Partners
collaborator INDUSTRY -
Nuvectra
lead INDUSTRY
Principal Investigators
-
Ben Tranchina · Nuvectra
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-06-30
- Primary Completion
- 2019-11-30
- Completion
- 2019-11-30
- FDA Device
- Yes
Countries
- United States
- Germany
Study Locations
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