Trials / Withdrawn
WithdrawnNCT00887835
A Post-Market Study of Transfacet Lumbar Spine Fixation and Fusion Utilizing the PERPOS™ PLS System
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Interventional Spine, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to utilize the PERPOS™ PLS System for transfacet lumbar spine fixation to evaluate its effect on patients' level of pain, procedural complications and functional status.
Detailed description
The PERPOS™ PLS System involves a minimally invasive, percutaneous implant procedure via a small incision. The PERPOS™ PLS is intended for lumbar bilateral facet fixation, with or without bone graft, at single or multiple levels from L1 to S1.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | PERPOS™ PLS | To stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. |
Timeline
- Start date
- 2009-04-01
- Primary completion
- 2010-10-01
- First posted
- 2009-04-24
- Last updated
- 2012-04-27
Source: ClinicalTrials.gov record NCT00887835. Inclusion in this directory is not an endorsement.