Actively Recruiting
Anatomic TSA Vs RTSA for Glenohumeral Arthritis
Led by La Tour Hospital · Updated on 2024-10-26
296
Participants Needed
1
Research Sites
265 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There are no published prospective studies that compared 2-year functional outcomes of RTSA and anatomic TSA for the treatment of primary glenohumeral osteoarthritis with intact rotator cuffs and no excessive glenoid retroversion. The primary goal of our prospective randomized study is to determine whether RTSA have at least as good results as anatomic TSA (non-inferiority), in patients with glenohumeral osteoarthritis, without rotator cuff tears nor significant glenoid retroversion.
CONDITIONS
Official Title
Anatomic TSA Vs RTSA for Glenohumeral Arthritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary glenohumeral arthritis
- Intact rotator cuff
- No significant glenoid bone loss
- Patients aged between 65 and 85 years
- Provided informed consent documented by signature
You will not qualify if you...
- B2 glenoid with >80% posterior humeral head subluxation or >25 degrees neoglenoid retroversion
- B3 and C type glenoids
- Full thickness rotator cuff tear
- Acute or malunited proximal humeral fracture
- Chronic locked dislocation
- Rheumatoid arthritis
- Revision surgery or previous shoulder surgery
- Tumors
- Axillary nerve damage
- Non-functioning deltoid muscle
- Glenoid vault deficiency preventing baseplate fixation
- Infection or neuropathic joints
- Known or suspected non-compliance, drug or alcohol abuse
- Incapable of judgment or under legal guardianship
- Inability to follow study procedures due to language, psychological disorders, dementia, or contraindication for CT scan
- Investigator or related persons' enrolment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
La Tour Hospital
Meyrin, Switzerland, 1217
Actively Recruiting
Research Team
A
Alexandre Lädermann, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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