Filter Results

Clinical Studies

Open

  • TORNIER PERFORM™ Stemless Reverse IDE Study (TORNIER PERFORM™ Stemless Reverse IDE Study) Rochester, Minn.

    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.

     

     

Contact Us for the Latest Status

  • Outcomes of Pectoralis Minor and Brachial Plexus Release Rochester, Minn.

    The purpose of this study is to to assess the clinical and radiographic outcomes of patients who have undergone shoulder arthroplasty.

  • Outcomes of Rotator Cuff Repair Rochester, Minn.

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

  • Outcomes of Shoulder Arthroplasty Rochester, Minn.

    The purpose of this study is to evaluate the outcomes and complications in patients who have received a hemiarthroplasty, anatomic total shoulder, or reverse total shoulder arthroplasty.

     

  • PERFORM™ HUMERAL SYSTEM STUDY (PHS) Rochester, Minn.

    The purpose of this study is to collect data needed to satisfy the European Union (EU) Medical Device Regulation (MDR) clinical post-market surveillance (PMS) and reporting requirements, and to support future regulatory submissions and peer-reviewed publications on device performance and safety.

     

  • Return to Sports After Reverse Total Shoulder Arthroplasty Rochester, Minn.

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

     

Closed for Enrollment

.