Total Knee Replacement With Duracon® and Vanguard™ Prostheses

NCT00588887 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2017-06-21

No results posted yet for this study

Summary

The purpose of this study is to compare range of motion, Knee Society Scores, and duration of surgery for different total knee prostheses.

Conditions

Interventions

DEVICE

Duracon®

This group utilizes the Duracon® prostheses for total knee replacement.

DEVICE

Vanguard™

This group will utilize the Vanguard™ prostheses for total knee replacement.

Sponsors & Collaborators

  • New Lexington Clinic

    collaborator OTHER
  • Biomet Orthopedics, LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-06-30
Primary Completion
2008-02-29
Completion
2008-06-30

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 NCT00588887 on ClinicalTrials.gov