Cementless Oxford Partial Knee Controlled Observational Study

NCT02350049 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 391

Last updated 2017-12-08

No results posted yet for this study

Summary

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

Conditions

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Prof. David Murray, BA Hons, BChir, FRCS, MD · Nuffield Orthopaedic Centre

  • Prof. Hemant Pandit, MBBS, MS, DNB, FRCS, DPhil · Nuffield Orthopaedic Centre

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2016-03-31
Completion
2017-04-30

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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 NCT02350049 on ClinicalTrials.gov