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Fixation and Range of Motion of the Reverse Shoulder Prosthesis

Fixation and Range of Motion of the Reverse Shoulder Prosthesis - Fixation and Range of Motion of the Reverse Shoulder Prosthesis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32621
Enrollment
10
Registered
2010-04-07
Start date
2011-03-01
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

rheuma rheumatoid arthritis

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Individuals requiring reverse arthroplasty as a result of rotator cuff tear arthropathy. • Rotator cuff tear, pre-operatively diagnosed by means of MRI. • Adequate bone stock glenoid visualized using CT. • Age > 70 years.

Exclusion criteria

Exclusion criteria: • Inadequate bone stock of glenoid. • Paresis or paralysis of the deltoid muscle. • Not capable of speaking Dutch. • Previous shoulder replacement surgery

Design outcomes

Primary

MeasureTime frame
Roentgen Stereophotogrammic Analysis Range of motion simulations and measurements

Secondary

MeasureTime frame
Functional Outcome Questionnaires

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)