MedTrace Logo

A Clinical Investigation of the Oxford® Meniscal Unicompartmental Knee System

NCT00578994 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 388

Last updated 2021-04-21

No results posted yet for this study

Summary

The purpose of this study is to collect information on complications and survivorship of patients implanted with the Oxford™ Meniscal Unicompartmental Knee System at multiple sites in the United States.

Conditions

Interventions

DEVICE

Oxford® Meniscal Unicompartmental Knee System

Oxford® Meniscal Unicompartmental Knee System is a medial, unicompartmental knee prosthesis containing three components: a femoral component, a tibial component, and a tibial meniscal bearing.

Sponsors & Collaborators

  • Biomet Orthopedics, LLC

    lead INDUSTRY

Principal Investigators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31
Primary Completion
2019-12-31
Completion
2021-03-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT00578994 on ClinicalTrials.gov