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A Clinical Investigation of the Copeland™ Humeral Resurfacing Head

NCT00698750 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 34

Last updated 2017-06-21

No results posted yet for this study

Summary

The purpose of this study is to perform a five-year, prospective evaluation of the Copeland™ Humeral Resurfacing Head Prosthesis for outcome and durability. Relief of pain and restoration of function will determine long-term clinical outcome while durability will be measured by the absence of revisions.

Conditions

Sponsors & Collaborators

  • Biomet Orthopedics, LLC

    lead INDUSTRY

Principal Investigators

  • Kenneth J Beres, MD · Director, Clinical Research, Biomet Orthopedics, LLC

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-04-30
Primary Completion
2009-11-30
Completion
2009-11-30

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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 NCT00698750 on ClinicalTrials.gov