Trials / Terminated
TerminatedNCT02068768
Multicenter Study of the Avenue L Interbody Spinal Fusion System Using VerteBRIDGE Plating and Posterior Fixation
A Prospective, Multicenter, Open Label Clinical Study of the Safety andEfficacy of the Avenue L Interbody Spinal Fusion System Using the VerteBRIDGE Plating System and Supplemental Posterior Fixation
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 13 (actual)
- Sponsor
- LDR Spine USA · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this prospective clinical study is to examine the short-term safety and efficacy of the Avenue®- L interbody Spinal Fusion System with VerteBRIDGE® plating to treat one and two level degenerative disc disease between L2 and S1 with a focus on fusion rate.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Avenue® L Interbody Fusion System (LDR Spine) | PEEK, intervertebral cage for interbody fusion of the lumbar spine |
Timeline
- Start date
- 2013-07-15
- Primary completion
- 2016-03-09
- Completion
- 2016-03-23
- First posted
- 2014-02-21
- Last updated
- 2019-07-05
- Results posted
- 2019-07-05
Locations
4 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02068768. Inclusion in this directory is not an endorsement.