Conjoint Tendon Resection for Frozen Shoulder
What You Need to Know Before You Apply
What is the purpose of this trial?
The trial aims to improve shoulder movements, particularly the ability to move the hand behind the back, in patients with shoulder issues often found after rotator cuff tear surgery. It compares standard shoulder surgery to a version where the conjoint tendon near the shoulder is cut (Conjoint Tendon Resection) to determine if this improves motion. This trial may suit individuals scheduled for their first reverse shoulder replacement surgery but not those undergoing a second surgery or dealing with a recent shoulder fracture. As an unphased trial, it offers a unique opportunity to contribute to innovative research that could enhance surgical outcomes for future patients.
Do I need to stop my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications.
What prior data suggests that conjoint tendon resection is safe for reverse total shoulder arthroplasty?
Research has shown that releasing the conjoint tendon, a treatment for frozen shoulder, can safely improve shoulder movement. Although specific safety data on this procedure is limited, studies suggest it effectively enhances shoulder rotation after surgery, indicating good patient tolerance.
The treatment involves carefully cutting the tendon to restore movement. Previous reports have not identified major safety issues, which is reassuring. However, discussing any personal health concerns with a healthcare provider before joining a trial is important.12345Why are researchers excited about this trial?
Researchers are excited about the Conjoint Tendon Resection for frozen shoulder because it offers a novel approach to treatment. Unlike standard treatments like physical therapy or corticosteroid injections, this technique involves a surgical modification during reverse total shoulder arthroplasty (RTSA). By releasing the conjoint tendon, the approach aims to enhance shoulder mobility and reduce pain. This direct intervention could significantly improve recovery outcomes compared to current methods, which often take longer to show results.
What evidence suggests that conjoint tendon resection during reverse total shoulder arthroplasty could be effective for improving functional internal rotation?
This trial will compare Reverse Total Shoulder Arthroplasty (RTSA) with and without Conjoint Tendon Resection. Research has shown that conjoint tendon resection can improve shoulder function in individuals with shoulder issues. One study found that patients who underwent this procedure reported better shoulder movement and less pain. Specifically, their pain levels dropped significantly, and their ability to use their shoulder nearly doubled after surgery. This suggests that releasing the tendon can help restore movement, particularly when turning the arm inward. While these results are promising, further research is needed to confirm its benefits specifically for frozen shoulder.678910
Are You a Good Fit for This Trial?
This trial is for patients who are having their first reverse total shoulder arthroplasty (RTSA), a type of shoulder replacement surgery. It's not open to those needing revision RTSA or RTSA due to an acute fracture or its after-effects.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo Reverse Total Shoulder Arthroplasty (RTSA) with or without conjoint tendon resection
Follow-up
Participants are monitored for safety and effectiveness after treatment, with assessments of functional internal rotation and various health scores
What Are the Treatments Tested in This Trial?
Interventions
- Conjoint Tendon Resection
Conjoint Tendon Resection is already approved in United States, European Union for the following indications:
- Improvement of functional internal rotation in patients undergoing reverse total shoulder arthroplasty
- Enhancement of postoperative functional internal rotation in reverse total shoulder arthroplasty patients
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Missouri-Columbia
Lead Sponsor