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A Comparison of Stryker's Tritanium Posterior Lumbar Cage and PEEK Implant

NCT03817606 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2023-01-10

Study results available
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Summary

The purpose of this study is to compare outcomes of patients with degenerative disc disease undergo lumbar spinal fusion with Stryker's Tritanium® Posterior Lumbar Cage or the UniLIF PEEK implant.

Conditions

  • Degenerative Disc Disease
  • Degenerative Scoliosis

Interventions

DEVICE

Tritanium Posterior Lumbar Cage

Placement of Tritanium Posterior Lumbar Cage via TLIF procedure

DEVICE

AVS UniLIF PEEK Posterior Lumbar Cage

Placement of AVS UniLIF PEEK Posterior Lumbar Cage via TLIF procedure.

Sponsors & Collaborators

  • Stryker Spine

    collaborator INDUSTRY

  • Riverside Medical Center

    lead OTHER

Principal Investigators

  • Lisa Zipsie · Riverside Medical Center

  • Juan Jimenez, MD · Riverside Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-01
Primary Completion
2020-06-30
Completion
2021-04-27
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT03817606 on ClinicalTrials.gov