Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty Outcomes
This study is looking at ways to prevent shoulder pain after a reverse shoulder replacement surgery (Reverse Shoulder Arthroplasty). Some people experience pain in the front of their shoulder because the surgery can put extra stress on a tendon called the conjoint tendon. This study will compare two surgical approaches: a standard reverse shoulder arthroplasty, and a reverse shoulder arthroplasty where the conjoint tendon is also lengthened. Researchers want to see if lengthening the conjoint tendon can reduce or prevent this pain one year after surgery. You may be able to join if you are at least 18 years old and are having your first reverse total shoulder arthroplasty at specific Loyola hospitals. The study plans to enroll 110 participants, but its current status is unclear.
- Study design
- This is an interventional study comparing two surgical procedures. It plans to enroll 110 participants.
- What's involved
- Participants will undergo either a standard reverse shoulder arthroplasty or a reverse shoulder arthroplasty with conjoint tendon lengthening. Your shoulder health will be assessed from enrollment until 12 months after treatment.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for 12 months after their treatment to assess their shoulder health.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Prophylactic Conjoint Tendon Lengthening During Reverse Shoulder Arthroplasty Outcomes
At a glance
Conditions
NCT06729983
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Loyola Outpatient Center
Maywood, Illinoisstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Nickolas G Garbis, MD · PRINCIPAL_INVESTIGATOR · Loyola University
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
Exclusion
What this trial measures
- American Society of Shoulder and Elbow Surgeons (ASES) ScoreFrom enrollment to the end of treatment at 12 months
The ASES is a 100-point scale that consists of two dimensions: pain and activities of daily living. There is one pain scale worth 50 points and ten activities of daily living worth 50 points. The higher the points the better the outcome.