Condition: Intervertebral Disc Degeneration · Sponsor: SPINEVISION SAS
The goal of this observational study is to confirm the safety and performance of the three (3) Spinevision posterior fixations systems Lumis®, Plus® and Ulis® , in the treatment of patient suffering from thoracolumbar spinal degenerative pathologies, or degenerative disc disease (disease that occurs when the spinal disk break down) associated pathologies. Part of their standard of care, participants will be questioned on their back and leg pains, their disability and if they have encountered any adverse effects since the Spinevision posterior fixation system implant surgery. Those data will be collected up to twenty four (24) months after the Spinevision posterior fixation system implant surgery.
This description comes directly from the study's public registry record.
Renaud Duchenes · +33 6 86 16 61 91 · r.duchenes@spinevision.com
Hanta Ranaivoson · h.ranaivoson@spinevision.com
Always discuss trial participation with your own doctor first.
| DOSCEA Pôle Rachis | Bayonne, France | Recruiting |
| Clinique du dos Bordeaux-Terrefort | Bruges, France | Recruiting |
| Orthéo Neurochirurgie | Saint-Etienne, France | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06342765