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Retrospective Encore Reverse Shoulder Prosthesis Study

NCT00765037 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 19

Last updated 2010-08-25

Study results available
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Summary

The purpose of this study is to evaluate the survivorship and efficacy of the Encore Reverse Shoulder Prosthesis in a group of no more than 50 subjects for whom data collection has already begun.

Conditions

  • Rotator Cuff Deficiency
  • Glenohumeral Arthritis

Interventions

DEVICE

Encore Reverse Shoulder Prosthesis

rotator cuff deficiency and glenohumeral arthritis

Sponsors & Collaborators

  • Encore Medical, L.P.

    lead INDUSTRY

Principal Investigators

  • J. Michael Kioschos, M.D. · Nashville Orthopedic Specialists

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2009-05-31
Completion
2009-05-31

Countries

  • United States

Study Locations

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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 NCT00765037 on ClinicalTrials.gov