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Trials / Completed

CompletedNCT02350049

Cementless Oxford Partial Knee Controlled Observational Study

Cementless Oxford Partial Knee Retrospective and Prospective Controlled Multi-center Observational Study

Status
Completed
Phase
Study type
Observational
Enrollment
391 (actual)
Sponsor
Zimmer Biomet · Industry
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety and effectiveness of the Cementless Oxford Partial Knee System.

Detailed description

The study is designed to document and compare the clinical and radiographic results of the Cementless Oxford Partial Knee System (investigational device) to those of the cemented Oxford Partial Knee System (control device).

Conditions

Timeline

Start date
2014-11-01
Primary completion
2016-03-01
Completion
2017-04-01
First posted
2015-01-29
Last updated
2017-12-08

Source: ClinicalTrials.gov record NCT02350049. Inclusion in this directory is not an endorsement.

Cementless Oxford Partial Knee Controlled Observational Study (NCT02350049) · Clinical Trials Directory