Actively Recruiting
Study of Personalized Instrument in Total Shoulder Arthroplasty The P.I.T.S.A. Study
Led by Université de Montréal · Updated on 2025-09-22
112
Participants Needed
1
Research Sites
477 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Total shoulder arthroplasty is an effective procedure to improve patients function and to relieve shoulder pain in cases of glenohumeral arthritis. The main challenge of this procedure is implanting the glenoid component. Indeed, surgical exposure is difficult and proper visualization of the glenoid is demanding. The current free-hand method is not precise and especially unreliable in glenoids with severe deformity. Inappropriate reaming and glenoid positioning can cause more bone loss during surgery. In anatomic prostheses, glenoid component fixation is demanding and is the first component to present loosening at long term follow-up. When it comes to reverse arthroplasty, the glenoid component, once again, requires the most attention. Malpositioning of the glenosphere can cause notching, loosening, and instability. In order to prevent these complications, precision in glenoid implantation is key. To this end, intraoperative computer navigation would be a helpful tool, but the increased expenses in computer equipment represent massive costs and possibly increases in surgical time. A more affordable option is a personalized guide, for which the only extra expense is the customized guide. These guides are based on precise 3D CT scan templates. Previous studies have evaluated the precision of the guide in vivo and in vitro, but none have measured it in a randomized study. As it represents additional costs, its efficacy needs to be proven before widespread use. This method may also provide secondary benefits, such as decreasing operating time, lowering short- and long-term complications, and improving efficacy. The objective of this study is to evaluate the performance of a patient specific glenoid guide.
CONDITIONS
Official Title
Study of Personalized Instrument in Total Shoulder Arthroplasty The P.I.T.S.A. Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with shoulder osteoarthritis and avascular necrosis (AVN)
You will not qualify if you...
- Patients with previous shoulder arthroplasty
- Patients with inflammatory arthritis or tumor
- Patients with previous shoulder surgery involving a metal implant
- Patients who refuse to participate in a 2-year follow-up
- Patients who do not speak English or French
- Patients with current or previous shoulder infection
- Patients who receive a graft during surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpital du Sacré-Cœur de Montréal
Montreal, Quebec, Canada, H4J 1C5
Actively Recruiting
Research Team
D
Dominique Rouleau, MD
CONTACT
K
Karine Tardif
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here