Expired Study
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Nashville, Tennessee 37203


Purpose:

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.


Criteria:

Inclusion Criteria: - The RSP is indicated for use in patients with a grossly rotator cuff deficient shoulder joint with severe arthropathy or a previously failed joint replacement with a grossly rotator cuff deficient shoulder joint. - The patient's joint must be anatomically and structurally suited to receive the selected implant(s), and a functional deltoid muscle is necessary to use the device. - The glenoid baseplate is intended for Cementless application with the addition of screws for fixation. The humeral stem is intended for cemented use only. Exclusion Criteria: - Infection or sepsis - Insufficient bone quality which may affect the stability of the implant, as determined by the physician - Muscular, neurological, or vascular deficiencies, which compromise the affected extremity - Alcoholism or other addictions - Materials (metals, etc) sensitivity - Loss of ligamentous structures - High levels of physical activity - Non-functional deltoid muscle


NCT ID:

NCT00765037


Primary Contact:

Principal Investigator
J. Michael Kioschos, M.D.
Nashville Orthopedic Specialists


Backup Contact:

N/A


Location Contact:

Nashville, Tennessee 37203
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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