Clinical Trials Logo

Clinical Trial Summary

The subscapularis is part of the rotator cuff and is release as part of a reverse shoulder replacement. The decision to repair this tendon is controversial. This research is being done to help determine if rotator cuff repair improves or hinders shoulder replacement. A worrisome but rare complication after shoulder replacement is dislocation. Rotator cuff repair may help reduce this risk. The repair may hinder some of the range of motion afterwards or could help with internal rotation strength. There is a chance that the repair doesn't matter at all. The goal of this study is to delineate outcomes after reverse shoulder arthroplasty with the respect to management of the subscapularis tendon. Further information about rotator cuff repair after reverse shoulder replacement can help define complications, potentially decrease OR time, and improve functional outcomes. A total of 148 patients will be enrolled and the duration of the study will be 5 years. All patients will be required to follow-up at 2¬-week, 6-week, 3-month, 6-month, 1-year, and 2-year post-operative marks. Any time information is collected for a study there is a small risk of breach of confidentiality. There are no monetary costs or payments associated with this study. You may or may not benefit by taking part in this study. There is no guarantee that you will receive direct benefit from your participation in this study. To be clear, participation in this study is completely voluntary.


Clinical Trial Description

You're going to undergo a procedure called a reverse shoulder replacement and I'm sure Dr. Gilotra already went over the procedure with you but I will again briefly. Before the hardware is put in, there is a tendon in your shoulder that has to be "released". It's released because the doctor has to move it out of the way to get to your shoulder joint. Now when the hardware has been implanted and the surgery is complete, the doctor now has two options. He can decide to repair this tendon or not. The thing is due to the hardware that is implanted, your shoulder doesn't really need this tendon anymore to help it move. So, there are some doctors in the country who choose to repair the tendon and there are some doctors who choose to just let it be. Patients have done great with either or. We are performing this nationwide study to see if one option (between repairing this tendon or leaving it) is slightly better than the other. There is a chance that repairing the tendon can decrease the risk of dislocations in the future and also help you move your arm better. There is a chance that this repair doesn't matter at all. If we figure out whether to repair or not to repair this tendon, we will be able to better define complications, potentially decrease surgery time, and improve how well patients perform daily activities. We randomize you to the repair on don't repair group, almost like flipping a coin. With me, you'll be answering simple questions that will track your functionality over time. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05344898
Study type Interventional
Source University of Maryland, Baltimore
Contact Mohit Gilotra, MD
Phone 3015024102
Email mgilotra@som.umaryland.edu
Status Recruiting
Phase N/A
Start date November 15, 2022
Completion date May 15, 2027

See also
  Status Clinical Trial Phase
Completed NCT06070493 - The Effects of Myofascial Release Technique N/A
Completed NCT04541953 - TeleRehabilitation Following Arthroscopic Rotator Cuff Repair N/A
Completed NCT04944446 - Myofascial Release in Shoulder Pathologies N/A
Recruiting NCT06112444 - Validity And Reliability Study Of The Turkish Version Of Short Western Ontario Rotator Cuff Index
Completed NCT04594408 - Tranexamic Acid to Improve Arthroscopic Visualization in Shoulder Surgery Phase 4
Active, not recruiting NCT04686396 - Demineralized Bone Matrix Rotator Cuff Study N/A
Recruiting NCT05988541 - Rotator Cuff Integrity and Clinical Outcomes 5 Years After Repair. N/A
Completed NCT04470167 - Phase 1/2 Clinical Study of TPX-115 in Patients With Partial-Thickness Rotator Cuff Tear Phase 1/Phase 2
Recruiting NCT05297305 - Onlay Versus Inlay Humeral Component in Reverse Total Shoulder Arthroplasty N/A
Completed NCT02528084 - The Effects of Yoga on Patients With Rotator Cuff Injuries N/A
Recruiting NCT05011331 - The Effect of a Custom Pillow on Sleep Quality in Patients With Nonoperative Rotator Cuff Syndrome N/A
Recruiting NCT04209504 - Evaluating Hemidiaphragmatic Paralysis With Prolonged Neural Blockade From an Interscalene Brachial Plexus Block
Completed NCT03967574 - Subacromial Corticosteroid Injections and tDCS in Rotator Cuff Tendinopathy N/A
Not yet recruiting NCT05906004 - Retrospective Data Collection and Prospective Clinical Investigation for the Augmentation or Reinforcement of the Rotator Cuff Using the Pitch-Patch
Completed NCT04952623 - Online Education to Improve the Management of Rotator Cuff Related Shoulder Pain N/A
Recruiting NCT04175184 - Inclusion of Mobilisation With Movement to an Exercise Programme in Rotator Cuff Related Pain N/A
Terminated NCT05215600 - Anaverseā„¢ Glenoid System and Its Instrumentation
Recruiting NCT05822414 - ESP vs STB for Pain and Diagraphragm Function for Shoulder Surgery N/A
Completed NCT04833244 - Automatic Multimodal Assessment of Occurrence and Intensity of Pain for Research and Clinical Use N/A
Completed NCT03982108 - Comparison of Two Arthroscopic Rotator Cuff Repair Techniques: Knot-tying Versus Knotless Suture-bridge Technique N/A