Clinical trial
Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery
NCT00295009 · Synthes USA HQ, Inc., Industry · Completed
Key facts
| NCT number | NCT00295009 |
|---|---|
| Title | Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery |
| Official title | A Multi-Center, Prospective, Randomized, Controlled Clinical Trial Comparing the Safety and Effectiveness of ProDisc to Spinal Fusion Surgery in the Treatment of Discogenic Pain Associated With DDD in the Lumbosacral Spine |
| Acronym | PDL |
| Lead sponsor | Synthes USA HQ, Inc., Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Spinal Diseases |
| Intervention type | Device, Procedure |
| Interventions | ProDisc, Spinal Fusion |
| Enrollment | 852 |
| Start date | Sep 1, 2001 |
| Primary completion | Apr 1, 2011 |
| Completion | Apr 1, 2011 |
| First posted | Feb 22, 2006 |
| Last update posted | Aug 6, 2014 |
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: