Comparison of the Aspen Device Versus Pedicle Screws for Supplemental Posterior Fixation in Lumbar Interbody Fusion

Authors
Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2012
The purpose of this clinical investigation is to evaluate the Aspen™ device compared to pedicle screw instrumentation for posterior fixation in the treatment of patients with degenerative disc disease and/or spondylolisthesis. The Aspen™ device will be compared to pedicle screw instrumentation in Oswestry Disability Index (ODI) improvement and success of fusion.
Epistemonikos ID: ac924fafb79cb1840a1c79af5ffefbd383ef516a
First added on: May 10, 2024