Comparing two surgical approaches for shoulder joint replacement
The Impact of Conjoint Tendon Resection on Functional Internal Rotation of the Shoulder Following Reverse Shoulder Arthroplasty: A Prospective, Randomized Clinical Trial
This study is testing a new surgical method for shoulder joint replacement to see if it helps patients move their shoulder better compared to the standard approach.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 64 (estimated) |
| Sex | All |
| Sponsor | University of Missouri-Columbia Academic / other |
| Locations | 1 site (Columbia, Missouri) |
| Trial ID | NCT05753904 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of a surgical technique called conjoint tendon resection during reverse total shoulder arthroplasty (RTSA) compared to the standard RTSA approach. It will involve 64 patients undergoing RTSA by a single surgeon, with a focus on measuring postoperative functional internal rotation as the primary outcome. Secondary outcomes will include various patient-reported scores and assessments of shoulder movement and complications. The study is designed as a prospective, randomized-controlled trial, where participants and assessors will know the intervention being performed.
Who should consider this trial
Good fit: Ideal candidates for this study are patients undergoing primary reverse total shoulder arthroplasty.
Not a fit: Patients who may not benefit include those requiring revision RTSA or those undergoing RTSA for acute fractures.
Why it matters
Potential benefit: If successful, this study could lead to improved functional internal rotation and overall patient satisfaction after shoulder joint replacement.
How similar studies have performed: While this approach is being tested in this trial, similar studies have not been widely reported, making this a novel investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria - All patients undergoing primary reverse total shoulder arthroplasty (RTSA) Exclusion criteria * Revision RTSA * RTSA for acute proximal humerus fracture or fracture sequela
Where this trial is running
Columbia, Missouri
- Missouri Orthopaedic Institute — Columbia, Missouri, United States (Recruiting)
Study contacts
- Study coordinator: Charles Gusho, MD
- Email: umhsorthoenroll@umsystem.edu
- Phone: 2622417944
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.