Fixation and Range of Motion of the Reverse Shoulder Prosthesis
Completed
- Conditions
- rheumarheumatoid arthritis10023213
- Registration Number
- NL-OMON32621
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
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
• Inadequate bone stock of glenoid.
• Paresis or paralysis of the deltoid muscle.
• Not capable of speaking Dutch.
• Previous shoulder replacement surgery
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Roentgen Stereophotogrammic Analysis<br /><br>Range of motion simulations and measurements</p><br>
- Secondary Outcome Measures
Name Time Method <p>Functional Outcome Questionnaires</p><br>
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What biomechanical factors influence osseointegration of reverse shoulder prostheses in rheumatoid arthritis patients?
How does reverse total shoulder arthroplasty compare to standard prostheses in restoring glenohumeral range of motion for rheumatic conditions?
Which inflammatory biomarkers (e.g., TNF-α, IL-6) correlate with postoperative functional outcomes in NL-OMON32621 participants?
What are the incidence rates of periprosthetic osteolysis or loosening in reverse shoulder prostheses for rheumatoid arthritis?
How do cemented vs. cementless fixation techniques affect long-term stability in reverse shoulder arthroplasty for rheumatic diseases?