Total Knee Replacement Using Simplex® or Cobalt™ Bone Cement

NCT00589485 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2017-06-21

No results posted yet for this study

Summary

The purpose of this study is to collect radiographic and clinical outcomes of total knee replacement using Simplex® or Cobalt™ Bone Cement.

Conditions

Interventions

DEVICE

Simplex® Bone Cement

This arm will utilize Simplex® Bone Cement in total knee replacement.

DEVICE

Cobalt™ Bone Cement

This arm utilizes Cobalt™ Bone Cement in total knee replacement.

Sponsors & Collaborators

  • New Lexington Clinic

    collaborator OTHER
  • Zimmer Biomet

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-11-30
Primary Completion
2006-11-30
Completion
2006-11-30

Countries

  • United States

Study Locations

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Entities

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 NCT00589485 on ClinicalTrials.gov