Clinical trial
Kineflex Artificial Disc System to Treat Degenerative Disc Disease (DDD)
NCT00292292 · SpinalMotion, Industry · Terminated
Key facts
| NCT number | NCT00292292 |
|---|---|
| Title | Kineflex Artificial Disc System to Treat Degenerative Disc Disease (DDD) |
| Official title | Clinical Study Protocol for the Investigation of the Kineflex Spinal System - a Pivotal Study in Continued Access Stage |
| Lead sponsor | SpinalMotion, Industry |
| Status | Terminated |
| Study type | Interventional |
| Conditions | Degenerative Disc Disease |
| Intervention type | Device |
| Interventions | Lumbar Artificial Disc, Charite Artificial Disc |
| Enrollment | 514 |
| Start date | Jan 1, 2005 |
| Primary completion | May 1, 2009 |
| Completion | Aug 1, 2013 |
| First posted | Feb 15, 2006 |
| Last update posted | Sep 13, 2013 |
| Countries | United States |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: