Condition: Discogenic Low Back Pain · Sponsor: Spinal Stabilization Technologies
This is a traditional feasibility study (TFS) study to evaluate the safety and effectiveness of the PerQdisc. The study is prospective, multicenter, and open label. After a screening period, qualified participants will be enrolled and treated with the PerQdisc. Patients will not be blinded to their treatment. Participants will then complete the safety follow-up period.
This description comes directly from the study's public registry record.
Molly Bond · 1-800-484-1588 · clinical@sstspine.com
Always discuss trial participation with your own doctor first.
| Hope Research Institute | Glendale, Arizona, United States | Withdrawn |
| The CORE Institute | Phoenix, Arizona, United States | Recruiting |
| HOPE Research Institute | Phoenix, Arizona, United States | Withdrawn |
| HonorHealth Research & Innovation Institute | Scottsdale, Arizona, United States | Recruiting |
| Axis Spine Center | Coeur d'Alene, Idaho, United States | Recruiting |
| Indiana Spine Group | Carmel, Indiana, United States | Recruiting |
| Spine Institute of Louisiana | Shreveport, Louisiana, United States | Recruiting |
| SonoSpine | Oklahoma City, Oklahoma, United States | Withdrawn |
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Source record: clinicaltrials.gov/study/NCT06860867