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Describes the nature of a clinical study. Types include:
The primary objective of this study is to collect and evaluate long-term clinical and radiographic outcomes data to better understand the safety and performance of shoulder arthroplasty over time.
Study statuses change often. Please contact us for help.
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The purpose of this study is to to assess the clinical and radiographic outcomes of patients who have undergone shoulder arthroplasty.
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The purpose of this study is to compare validated clinical and functional outcomes between patients who acutely present with 3- and 4-part Proximal Humerus Fractures (PHFs) treated nonoperatively or with rTSA. We hypothesize that in displaced 3- and 4-part proximal humerus fractures, rTSA will have better pain relief and functional outcomes than nonoperative treatment.
The purpose of this study is to evaluate the outcomes and complications of anatomic total shoulder and reverse total shoulder arthroplasty systems.
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.
The purpose of the study is a multi-center prospective registry to collect clinical outcomes of anatomic and reverse total shoulder arthroplasty.
The purpose of this study is to to determine the impact of anesthesia (liposomal bupivacaine) on diaphragm muscle forces using a non-invasive ultrasonographic shear wave elastography (SWE) method.
The purpose of this study is to:
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