Clinical trial
Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion…
NCT00254852 · Exactech, Industry · Terminated
Key facts
| NCT number | NCT00254852 |
|---|---|
| Title | Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft |
| Official title | A Single Blind, Multi-Center, Randomized, Prospective Clinical Study Comparing Optecure™ Autograft Extender to Autograft Only in Fusion of the Lumbar Spine |
| Lead sponsor | Exactech, Industry |
| Status | Terminated |
| Study type | Interventional |
| Conditions | Stenosis, Spondylolisthesis, Degenerative Disc Disease |
| Intervention type | Procedure |
| Interventions | Posterior Lateral Fusion (PLF), Anterior Lumbar Interbody Fusion (ALIF), Transforaminal lumbar interbody fusion (TLIF), Posterior lumbar interbody fusion (PLIF), Extreme lateral interbody fusion (XLIF) |
| Enrollment | 94 |
| Start date | Oct 1, 2005 |
| Primary completion | Aug 1, 2011 |
| Completion | Aug 1, 2011 |
| First posted | Nov 17, 2005 |
| Last update posted | Nov 21, 2013 |
| Countries | United States |
At a glance
- 1–9 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: