A Multi-Site Study of the Zyga GlyDer Facet Restoration Device In Subjects With LUmbar FacET Pain Syndrome - DUET
Stopped early · Not applicable
Conditions studied: Facet Joint Pain
In brief
A non-randomized, multi-site feasibility study to evaluate the safety of the Glyder Device in subjects with a history of lumbar facet joint disease (L2 to the sacrum) and successful neural ablation in which the facet joint is confirmed as the source of pain.
Key facts
- Study ID
- NCT02179476
- Run by
- Zyga Technology, Inc.
- People needed
- 2
- Starts
- 2014-06-01
- Expected to finish
- 2018-09-01
- Last updated by the study team
- 2018-10-11
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- The Spine Institute — Santa Monica, California, United States
- Laser Spine Institute — Tampa, Florida, United States
- Clinical Radiology of Oklahoma — Edmond, Oklahoma, United States
- Northwest Orthopaedic Specialists — Spokane, Washington, United States
Full record on ClinicalTrials.gov
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