Trials / Completed
CompletedNCT00758719
Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion System
A Prospective Multicenter Lumbar Spine Fusion Study to Evaluate the Effectiveness of the Biomet Lumbar Spinal Fusion System
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 53 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the effectiveness of the Biomet Lumbar Spinal Fusion System in patients undergoing lumbar fusion surgery.
Detailed description
All subjects enrolled in this study will receive the The Biomet Osteobiologic Treatment System which is comprised of the SpF® Spine Fusion Stimulator and any or all of the following can be utilized in the study: any Pedicle Screw System, autograft and an Interbody Spacer
Conditions
Timeline
- Start date
- 2008-09-01
- Primary completion
- 2012-08-01
- Completion
- 2012-08-01
- First posted
- 2008-09-25
- Last updated
- 2020-02-24
Locations
4 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00758719. Inclusion in this directory is not an endorsement.