Resurfacing schouder prothese, radiologische en klinische follow up

The Copeland Hemiprothesis Extended Effectiveness Study and Evaluation

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON24598

Enrollment

Registered

2013-07-18

Start date

2013-07-22

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

primary osteoarthritis shoulder Hemiprothesis Copeland radiological clinical

Interventions

The Copeland Hemiprothesis

Eligibility

Inclusion criteria

Inclusion criteria: Primary glenohumeral osteoarthritis, intact rotator cuff, follow-up of at least 5 years and provision of consent

Exclusion criteria

Exclusion criteria: Preoperative diagnosis other than primary osteoarthritis (e.g. rheumatoid arthritis, instability arthropathy, post-traumatic arthropathy and avascular necrosis) and no provision of consent. Patients who where unable to complete the PROMs were excluded from clinical evaluation

Design outcomes

Primary

Measure	Time frame
Shoulder function: Constant score DASH score Simple Shoulder Test (SST)	—

Secondary

Measure	Time frame
Pain, quality of life and patient satisfaction: Visual Analogue Scale (VAS) EuroQol-5D questionnaire	—

Contacts

Public ContactM.G.M. Schotanus

Department of Orthopedic Surgery, Orbis Medisch Centrum dr H vd Hoffplein 1

m.schotanus@zuyderland.nl+31 (0)88 4597823

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)