Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
Last updated on July 2021Recruitment
- Recruitment Status
- Terminated
- Estimated Enrollment
- 63
Summary
- Conditions
- Spondylolisthesis
- Type
- Observational
- Design
- Observational Model: CohortTime Perspective: Prospective
Participation Requirements
- Age
- Between 50 years and 80 years
- Gender
- Both males and females
Description
Evaluate the clinical outcomes of subject with spondylolisthesis undergoing posterolateral fusion (PLF) surgery utilizing the Aspen™ Spinous Process Fixation System. The Aspen™ device will be evaluated using Oswestry Disability Index (ODI) improvement and success of fusion.
Evaluate the clinical outcomes of subject with spondylolisthesis undergoing posterolateral fusion (PLF) surgery utilizing the Aspen™ Spinous Process Fixation System. The Aspen™ device will be evaluated using Oswestry Disability Index (ODI) improvement and success of fusion.
Tracking Information
- NCT #
- NCT01560273
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Shah Goodman Campbell brain and Spine
Get Well Soon