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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00007556

Enrollment

Registered

2015-01-09

Start date

2007-02-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M19.01 T84.1

Interventions

Group 1: all implanted RSA of the new generation were pre-op, 1, 5 and 10 years after operation were evaluated using Constant score, clinical examination, force meassurement. radiologic controls were

Eligibility

Sex/Gender

All

Inclusion criteria

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

Exclusion criteria: death, not reached

Design outcomes

Primary

Measure	Time frame
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.	—

Countries

Germany

Contacts

Public ContactStephanie Gruber

St. VInzenz Klinik Pfronten

stephanie.gruber@vinzenz-klinik.de01608185941

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026