Clinical trial
A Safety and Efficacy Study for Treatment of Painful Vertebral Compression…
NCT00290862 · Orthovita d/b/a Stryker, Industry · Unknown status
Key facts
| NCT number | NCT00290862 |
|---|---|
| Title | A Safety and Efficacy Study for Treatment of Painful Vertebral Compression Fractures Caused by Osteoporosis |
| Official title | A Randomized, Controlled Clinical Study to Evaluate the Safety and Effectiveness of CORTOSS® Synthetic Cortical Bone Void Filler in Vertebral Augmentation |
| Lead sponsor | Orthovita d/b/a Stryker, Industry |
| Status | Unknown status |
| Study type | Interventional |
| Conditions | Spinal Fractures |
| Intervention type | Device |
| Interventions | Percutaneous Vertebral Augmentation of compression fractures |
| Enrollment | 256 |
| Start date | Sep 1, 2004 |
| Completion | Mar 1, 2009 |
| First posted | Feb 13, 2006 |
| Last update posted | Oct 15, 2008 |
| Countries | United States |
At a glance
- 10–99 Study sites
- No 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: