Clinical trial
Safety and Efficacy Study Comparing ProDisc-C to ACDF Surgery to Treat SCDD
NCT00291018 · Synthes USA HQ, Inc., Industry · Completed
Key facts
| NCT number | NCT00291018 |
|---|---|
| Title | Safety and Efficacy Study Comparing ProDisc-C to ACDF Surgery to Treat SCDD |
| Official title | A Multi-Center, Prospective, Randomized, Controlled Clinical Trial Comparing the Safety and Effectiveness of ProDisc-C to Anterior Cervical Discectomy and Fusion (ACDF) Surgery in the Treatment of Symptomatic Cervical Disc Disease (SCDD) |
| Lead sponsor | Synthes USA HQ, Inc., Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Symptomatic Cervical Disc Disease |
| Intervention type | Device |
| Interventions | Total Disc Replacement, ACDF |
| Enrollment | 368 |
| Start date | Aug 1, 2003 |
| Primary completion | Mar 1, 2015 |
| Completion | Mar 1, 2015 |
| First posted | Feb 13, 2006 |
| Last update posted | Nov 20, 2017 |
At a glance
- Yes Results posted
- 1–9 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: