NCT00791180

Posterior Lateral Fusion (PLF) With Dynesys

Clinical Outcomes Following Posterior Lateral Fusion With the Dynesys(R) Spinal System

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 38 (actual)
• Sponsor: Zimmer Biomet · Industry
• Sex: All
• Age: 20 Years – 80 Years
• Healthy volunteers: Not accepted

Summary

The primary purpose of this study is to track and document the clinical outcomes of patients with radicular pathology following posterior lateral fusion with the Dynesys Spinal System. Secondary purpose of this study is to assess outcomes with historical controls along a continuum of motion and anatomy sparing procedures.

Detailed description

This study will help the patient to the extent that it will allow the comparison of this unique treatment to the corpus of literature on radicular pathology, thus focusing a specific treatment for a specific pathology.

Conditions

• Spondylolisthesis

Timeline

• Start date: 2006-03-01
• Primary completion: 2011-03-01
• Completion: 2011-03-01
• First posted: 2008-11-14
• Last updated: 2011-09-29

Locations

1 site across 1 country: United States