Trials / Terminated
TerminatedNCT00878579
Percutaneous Dynamic Stabilization (PDS) System Versus Fusion for Treating Degenerative Disc Disease
A Study to Evaluate the Safety and Effectiveness of the PDS System to Treat Back Pain Associated With Degenerative Disc Disease
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Interventional Spine, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate the safety and effectiveness of the PDS System compared to the surgical control of posterolateral fusion with autograft and pedicle screw fixation for the treatment of one or two levels from L3-S1 to relieve back pain associated with degenerative disc disease.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | PDS System | Percutaneous Dynamic Stabilization System |
| DEVICE | Fusion | Transforaminal Interbody Fusion (TLIF) with Autograft and Pedicle Screws |
Timeline
- Start date
- 2009-03-01
- Primary completion
- 2013-02-01
- Completion
- 2013-02-01
- First posted
- 2009-04-09
- Last updated
- 2013-02-21
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00878579. Inclusion in this directory is not an endorsement.