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Clinical Trials/ACTRN12616000232437
ACTRN12616000232437
Completed
未知

Medium-term clinical and radiographic outcome of DePuy Delta Xtend reverse TSA at a minimum 5 year follow-up

DePuy International Ltd0 sites68 target enrollmentFebruary 19, 2016
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Conditionsshoulder arthritis associated with rotator cuff tearpost traumatic shoulder arthritis with rotator cuff tearmassive irreparable rotator cuff tear with or without arthritisMusculoskeletal - OsteoarthritisMusculoskeletal - Other muscular and skeletal disordersSurgery - Other surgery

Overview

Phase
未知
Intervention
Not specified
Conditions
shoulder arthritis associated with rotator cuff tear
Sponsor
DePuy International Ltd
Enrollment
68
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 19, 2016
End Date
December 22, 2017
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
DePuy International Ltd

Eligibility Criteria

Inclusion Criteria

  • •Retrospective analysis of a consecutive series of prospectively enrolled patients following reverse TSA for a variety of indications using the DePuy Delta Xtend reverse RSA system.

Exclusion Criteria

  • •Patients excuded if surgery not carried out by pre\-designated surgeon, if a conventional TSA or other form of arthroplasty rather than a reverse TSA was performed, or if an alternative implant was used for the procedure.

Outcomes

Primary Outcomes

Not specified

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