TSA vs RSA in Glenohumeral Osteoarthritis
Launched by OTTAWA HOSPITAL RESEARCH INSTITUTE · Jan 13, 2020
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is comparing two types of shoulder surgery—total shoulder arthroplasty (TSA) and reverse shoulder arthroplasty (RSA)—to see which option is better for older patients with shoulder osteoarthritis. Osteoarthritis is a condition that causes pain and stiffness in the joints, and this study is focusing on patients who are 65 years and older and have already tried other treatments for at least six months without relief. To qualify, participants need to have significant wear and tear in the cartilage of their shoulder, and their shoulder joint must have a specific alignment issue called glenoid retroversion.
If you or a loved one is over 65 and struggling with shoulder pain that hasn’t improved with medication, physical therapy, or lifestyle changes, you might be eligible to participate in this study. Participants will receive one of the two surgical treatments and will be monitored over time to see how well they recover and manage their pain. It's important to note that individuals with certain conditions, like infections or previous shoulder surgeries, may not be able to join. This trial aims to help find the best surgical approach for older adults facing these shoulder challenges.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- 1. Patients who have failed standard non-surgical management of their idiopathic shoulder osteoarthritis who would benefit from a shoulder arthroplasty. Failed medical management will be defined as persistent pain and disability despite adequate standard non-operative management for 6 months. Medical management will be defined as:
- • 1. The use of drugs including analgesics and non-steroidal anti-inflammatory drugs
- • 2. Physiotherapy consisting of stretching, strengthening and local modalities (ultrasound, cryotherapy, etc.)
- • 3. Activity modification
- • 2. Imaging, and intra-operative findings confirming advanced glenohumeral cartilage loss
- • 3. Patients may present with a glenoid deficiency and \</=15 degrees of retroversion
- • 4. 65 years of age and older
- Exclusion Criteria:
- • 1. Active joint or systemic infection
- • 2. Rotator cuff arthropathy
- • 3. Significant muscle paralysis
- • 4. Charcot's arthropathy
- • 5. Major medical illness (life expectancy less than 1 year or unacceptably high operative risk)
- • 6. Unable to understand the consent form/process
- • 7. Pregnancy
- • 8. Psychiatric illness that precludes informed consent
- • 9. Unwilling to be followed for the duration of the study
- • 10. Retroversion cannot be surgically corrected to within 10 degrees of neutral
- • 11. History of previous shoulder surgery on affected side
About Ottawa Hospital Research Institute
The Ottawa Hospital Research Institute (OHRI) is a leading academic research institute dedicated to advancing health and healthcare through innovative research and evidence-based practices. Affiliated with The Ottawa Hospital and the University of Ottawa, OHRI fosters a collaborative environment that brings together clinicians, scientists, and trainees to conduct groundbreaking clinical trials and translational research. With a focus on improving patient outcomes, OHRI specializes in a wide range of fields, including cancer, cardiovascular health, and regenerative medicine. The institute is committed to ethical research practices and the dissemination of knowledge to enhance public health and inform healthcare policy.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Ottawa, Ontario, Canada
Edmonton, Alberta, Canada
Winnipeg, Manitoba, Canada
Kingston, Ontario, Canada
Patients applied
Trial Officials
Peter Lapner, MD
Principal Investigator
The Ottawa Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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