MedTrace Logo

Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis

NCT01560273 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2019-01-09

No results posted yet for this study

Summary

The purpose of this clinical investigation is to 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.

Conditions

  • Spondylolisthesis

Interventions

DEVICE

Aspen Spinous Process Fixation Device

The Aspen device will be placed as posterior fixation to Posterolateral Fusion (PLF)

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Shah · Goodman Campbell brain and Spine

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2015-09-30
Completion
2015-09-30

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01560273 on ClinicalTrials.gov