Clinical Trials

The purpose of this study is to evaluate the outcomes and complications of anatomic total shoulder and reverse total shoulder arthroplasty systems using bone preserving shoulder arthroplasty system.

The purpose of this study is to determine whether a diagnostic reconciliation conversation aid can assist a shared decision-making conversation between patients and clinicians to reach a consensual diagnostic plan of care and confirm that patients and clinicians have the same understanding of its goals, nature (including patient experience), and downstream consequences (including implications for further testing and treatment).

The purpose of this study is to compare pain and function in patients undergoing operative versus non-operative treatment of atraumatic rotator cuff tears at 12 months of follow-up, and to assess effects of rotator cuff tear size and age on comparative outcomes of operative versus non-operative treatments for atraumatic rotator cuff tears.

The purpose of this study is evaluate the outcomes and complications in patients who underwent a rotator cuff repair.

The purpose of this study is to evaluate safety and efficacy and show non-inferiority of the investigational PERFORM Stemless Reverse device to the control PERFORM Stem Reverse device in subjects who are candidates for the treatment of noninflammatory degenerative joint disease (i.e., osteoarthritis), avascular necrosis, pseudoparalysis or anterior superior escape, rotator cuff tear arthropathy, correction of functional deformity, and post-traumatic arthritis.