MedTrace Logo

PEEK and Allograft Spacers Evaluation in Spinal Fusion Surgeries

NCT01406405 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 240

Last updated 2019-02-27

No results posted yet for this study

Summary

Purpose The primary purpose of this study is to prospectively compare clinical and radiographic clinical outcomes in patients undergoing cervical or lumbar interbody fusions and randomized to receive either polyetheretherketone (PEEK) or cortical allografts.

Conditions

  • Degenerative Disc Disease

Interventions

PROCEDURE

Posterior/Transforaminal Lumbar Interbody Fusion (P/TLIF), Anterior Cervical Discectomy and Fusion (ACDF)

Lumbar or cervical fusion

Sponsors & Collaborators

  • Justin Parker Neurological Institute

    lead OTHER

Principal Investigators

  • Alan T Villavicencio, MD · Boulder Neurosurgical Associates

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2018-05-16
Completion
2018-05-16

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 NCT01406405 on ClinicalTrials.gov