Clinical trial
Use of Spinal Sealant System During Spinal Surgery
NCT00458354 · M.D. Anderson Cancer Center, Other · Completed
Key facts
| NCT number | NCT00458354 |
|---|---|
| Title | Use of Spinal Sealant System During Spinal Surgery |
| Official title | A Prospective, Multi-Center, Randomized Controlled Study to Compare the Spinal Sealant System as an Adjunct to Sutured Dural Repair With Standard of Care Methods During Spinal Surgery |
| Lead sponsor | M.D. Anderson Cancer Center, Other |
| Collaborators | Confluent Surgical Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Spine Surgery, Excessive Repair, Spinal Cord Injuries, Complication of Surgical Procedure |
| Intervention type | Device, Procedure |
| Interventions | Spinal Sealant, Standard Methods of Closing of the Dura |
| Enrollment | 3 |
| Start date | Jan 1, 2006 |
| Primary completion | Nov 1, 2007 |
| Completion | Dec 1, 2008 |
| First posted | Apr 10, 2007 |
| Last update posted | Oct 12, 2011 |
| Countries | United States |
At a glance
- 1–9 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: