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Clinical Outcome Comparison Between Medial and Lateral Offset Reverse Shoulder Arthroplasty

NCT01086202 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 37

Last updated 2016-09-15

No results posted yet for this study

Summary

The purpose of this study is to prospectively evaluate two FDA approved implant designs for the Tornier Reverse Shoulder arthroplasty. The small difference in design is the amount of offset each implant has. This offset may improve clinical outcomes in the patient population. There have been no clinical comparative studies between these two designs in the literature to date. We would like to follow these patients for two years after implantation of the reverse shoulder and evaluate their radiographs, pain scores, and shoulder functional scores. this would be the first randomized prospective single blinded study of its kind.

Conditions

  • Rotator Cuff Tear
  • Proximal Humerus Fractures
  • Malunions
  • Chronic Proximal Humerus Dislocations

Sponsors & Collaborators

  • Loma Linda University

    lead OTHER

Principal Investigators

  • Wesley Phipatanakul, MD · Loma Linda University Health Dept. Orthopaedic Surgery

Eligibility

Min Age
50 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2014-09-30
Completion
2014-10-31

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 NCT01086202 on ClinicalTrials.gov