Clinical trial
Safety and Efficacy Study of Healos as a Bone Replacement to Treat Degenerative…
NCT00316121 · Advanced Technologies and Regenerative Medicine, LLC (ATRM), Other · Completed
Key facts
| NCT number | NCT00316121 |
|---|---|
| Title | Safety and Efficacy Study of Healos as a Bone Replacement to Treat Degenerative Disc Disease |
| Official title | A Prospective, Multicenter, Randomized Study Comparing the Use of HEALOS® to Autograft in a Transforaminal Lumbar Interbody Fusion (TLIF) Approach |
| Lead sponsor | Advanced Technologies and Regenerative Medicine, LLC (ATRM), Other |
| Collaborators | DePuy Spine Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Degenerative Disc Disease |
| Intervention type | Device |
| Interventions | HEALOS and Leopard Cage, Leopard Cage and Autograft |
| Enrollment | 138 |
| Start date | Apr 1, 2006 |
| Primary completion | Jan 1, 2010 |
| First posted | Apr 20, 2006 |
| Last update posted | Mar 3, 2011 |
| Countries | United States |
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: