Massive Rotator Cuff Tear Reconstruction
Rotator Cuff Tear ArthropathyTo compare bridging reconstruction to superior capsular reconstruction using human dermal allograft augmentation for repair of massive rotator cuff tears.
Impact of Humeral Component Version on Outcomes Following RTSA
Rotator Cuff Tear ArthropathyThe proposed study is a prospective, single-blinded, randomized trial to investigate the impact of humeral component version on shoulder range of motion and patient reported functional outcomes following reverse total shoulder arthroplasty.
Clinical and Radiological Outcomes of Medacta Shoulder System FR
Primary OsteoarthritisSecondary Osteoarthritis5 moreThis is a post-marketing surveillance on Medacta Shoulder System
Exactech Shoulder Post Market Clinical Follow-up Study
Osteo Arthritis ShouldersOsteonecrosis7 moreThe objective of this study is to collect and evaluate long-term clinical and radiographic outcomes data in order to better understand the safety and performance of the shoulder arthroplasty over time. This study will follow subjects long-term for a minimum of 10-years, without an early-term restriction on the amount of time they will be followed.
Clinical and Radiological Outcomes of Medacta Shoulder System (BE)
Primary OsteoarthritisSecondary Osteoarthritis5 moreThis is a post-market surveillance study on Medacta Shoulder System
TESS V3 Modular Total Shoulder System PMCF
Osteoarthritis ShoulderRheumatoid Arthritis9 moreThis is a multicenter, retrospective and prospective, non-controlled post market surveillance study. The objectives of this study are to confirm safety, performance and clinical benefits of the T.E.S.S.® Version 3 Anatomic and Reverse Modular Total shoulder prosthesis and its instrumentation.
Follow-up Evaluating Clinical and Radiological Outcomes of Total Shoulder Arthroplasty With Permedica's...
Cuff Tear ArthropathyPrimary Osteoarthritis7 moreThis observational study is conducted in order to evaluate the effectiveness of the primary total shoulder arthroplasty with the Permedica's MIRAI Modular Shoulder Prosthesis System on the general population of patients who are about to undergo this surgery for every indication. Patients requiring a revision shoulder arthroplasty will not be enrolled. The effectiveness will be evaluated in terms of recovery of shoulder function and stability of the prosthetic implant. The incidence of complications, adverse and serious adverse events will also be studied. Additional study aim is to evaluate a medium/long term survival of the prosthesis. The duration of the study per single subject is 5 years.
Clinical and Radiological Outcomes of Medacta Shoulder System
Primary OsteoarthritisSecondary Osteoarthritis5 moreThis is a post-marketing surveillance on Medacta Shoulder System
Impact of Glenosphere Size on Range of Motion in Female Patients Undergoing Reverse Shoulder Arthroplasty...
Rotator Cuff Tear ArthropathyMassive Irreparable Rotator Cuff TearThe purpose of this study is to perform a prospective randomized trial among female patients undergoing reverse shoulder arthroplasty (RSA) to determine if a larger glenosphere allows greater range of motion without an impact on complications.
Cutibacterium Acnes in Deep Tissues in Primary Spine and Shoulder Surgery
Rotator Cuff Tear ArthropathySpine DegenerationObtain deep tissue samples from patients undergoing primary prosthetic surgery of the shoulder and patients undergoing primary instrumented surgery of the spine. Patients will be randomized to receive benzoyl peroxide 3 days prior to surgery.