5 year follow-up after reverse shoulder arthroplasty (RSA) of the new generation (Delta XTEND)

• Conditions: M19.01; T84.1; Mechanical complication of internal fixation device of bones of limb

• Registration Number: DRKS00007556
• Lead Sponsor: St. Vinzenz- Klinik Pfronten

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-01-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 49

Inclusion Criteria

Implantation of a RSA in
1. Cuffarthropathy
2. Omarthrosis wth RC-tears,
3. post-traumat. arthrosis with Rotatorcuff insufficiency
4. Problem depending on ohter kind of Implant

Exclusion Criteria

death, not reached

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
baseline, 1, 5 and 10 years after operation, CMS (pre and 1 year post-op through validated german questionnaire, after 5 years clinical score with force measurement). In addition the SST is acquired via questionnaire. Satisfaction was asked with school marks (1-6). X-ray controls were taken pre- and 1 year post-op standardised. After 5 years, patients could decide to get a voluntary xray.