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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON56120

Enrollment

Registered

2021-04-26

Start date

2021-08-06

Completion date

Unknown

Last updated

2024-12-02

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

Conditions

degenerative shoulder complaints wear and tear shoulder

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria: - Inability to understand written or verbal Dutch language

Design outcomes

Primary

Measure	Time frame
The accuracy of the positioning of the glenoid component, measured on a CT-scan	—

Secondary

Measure	Time frame
Position of the prothesis Range of motion Adverse events PROMs: NRS, DASH, Constant Murley score, Oxford shoulder test, EQ-5D Additional costs of surgery (planning)	—

Countries

Netherlands

Outcome results