RecruitingNCT04529798
Clinical Study Evaluating Outcomes of Reverse Shoulder Arthroplasty With SMR Stemless
A Monocentric Clinical Study Evaluating Clinical and Patient-reported Outcomes of Reverse Shoulder Arthroplasty With SMR Stemless
Sponsor
Arthro Medics AG
Enrollment
60 participants
Start Date
Nov 22, 2016
Study Type
OBSERVATIONAL
Conditions
Summary
The objectives of this study are the assessment of the clinical, radiographical and patient-reported outcomes of SMR Stemless Reverse Shoulder Arthroplasty (LimaCorporate S.p.A.) used as standard of care over a period of at least 2 years of follow-up and the evaluation of the incidence of any complication.
Eligibility
Min Age: 18 Years
Inclusion Criteria2
- rotator-cuff arthropathy, osteoarthritis
- approving written informed consent
Exclusion Criteria3
- Female patients who are pregnant, nursing, or planning a pregnancy.
- All adult patients with any of the SMR Stemless contraindication for use for the reverse configuration as reported in the current local Instruction for use.
- not consenting in participating in this study
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04529798
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