NCT02014350UnknownNot Applicable
Outcomes Following Delta Xtend Reverse Shoulder System
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Locations
- 1
- Primary Endpoint
- Implant Survivorship
Study Overview
Brief Summary
To collect medium to long-term survivorship implant outcomes on the DePuy Delta Xtend Reverse Shoulder Stystem.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Cross Sectional
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients whom were implanted with the DePuy Delta Xtend Reverse Total Shoulder System in the time frame indicated. Patients must be willing to sign the consent form and complete all follow-up visits.
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Implant Survivorship
Time Frame: 10 years post-operative
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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