Improvement of glenoid component positioning using patient specific instrumentation in reverse shoulder arthroplasty

Completed

• Conditions: degenerative shoulder complaints; wear and tear shoulder; 10023213; 10005944

• Registration Number: NL-OMON56120
• Lead Sponsor: Viecuri Medisch Centrum voor Noord-Limburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 94

Inclusion Criteria

- Scheduled for a reverse shoulder arthroplasty (for one of the following
indications:
rotator cuff tear arthropathy; irreparable rotator cuff tear, osteoarthritis,
rheumatoid artritis) according to the freehand or 5D method.
- Provide written informed consent

Exclusion Criteria

- Inability to understand written or verbal Dutch language

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The accuracy of the positioning of the glenoid component, measured on a CT-scan</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Position of the prothesis<br /><br>Range of motion<br /><br>Adverse events<br /><br>PROMs: NRS, DASH, Constant Murley score, Oxford shoulder test, EQ-5D<br /><br>Additional costs of surgery (planning)</p><br>