Clinical trial
Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™…
NCT00095095 · Medtronic Spinal and Biologics, Industry · Terminated
Key facts
| NCT number | NCT00095095 |
|---|---|
| Title | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™ Fusion Device |
| Official title | Lumbar Interbody Fusion Using The Telamon® Peek™ Versus The Telamon® Hydrosorb™ Fusion Device - A Prospective, Randomized Controlled Trial To Assess Surgical And Clinical Outcomes |
| Lead sponsor | Medtronic Spinal and Biologics, Industry |
| Status | Terminated |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Low Back Pain, Spondylolisthesis, Spinal Stenosis, Intervertebral Disc Displacement |
| Intervention type | Device |
| Interventions | Lumbar Interbody Fusion |
| Enrollment | 102 |
| Start date | Oct 1, 2004 |
| Completion | May 1, 2006 |
| First posted | Nov 1, 2004 |
| Last update posted | Feb 13, 2018 |
| Countries | Germany, Netherlands |
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: