[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"rotator-cuff-tear-arthropathy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:rotator-cuff-tear-arthropathy":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,50,80,106,135,160,189,213,239],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100628694","emg-and-delta-function-in-standard-rtsa-vs-lateralization-100628694",false,"NCT07464977","EMG and Delta Function in Standard RTSA vs Lateralization","Postoperative Deltoid EMG Activity and Function in Patients After Reverse Total Shoulder Arthroplasty: A Comparison of Standard Implantation Technique and Lateralization","EMGRTSA","Inclusion Criteria:\n\n* male\u002Ffemale, 60-85y\n* diagnosis of Cuff tear arthropathy (CTA)\n* irreparable rotator cuff tear\n* severe osteoarthritis (OA)\n* primary RSA\n* verified rotator cuff tear in preoperative MRI\n* absence of severe cognitive impairment\n\nExclusion Criteria:\n\n* previous muscle transfer\n* revision surgery\n* highly dysplastic glenoid\n* axillary nerve palsy\n* upper limb radiculopathy\n* cervical myelopathy\n* degenerative muscular disease,\n* previous proximal humeral fracture\n* revision arthroplasty\n* rheumatoid arthritis","ALL","60 Years","85 Years",{"count":21,"type":22},130,"ESTIMATED","INTERVENTIONAL",[25],"NA","Reverse total shoulder arthroplasty (RTSA) is a well-established method to treat patients with irreparable rotator cuff tears and glenohumeral osteoarthritis. The biomechanical principle implies a medialization and distalization of the center of rotation (COR). Deficiencies in internal and external rotation constitute frequently encountered functional problems. Some studies showed reduced activation of the posterior deltoid in EMG measurements, which may explain the inability to compensate these movements. Lateralized prosthetic designs demonstrated increased external rotation through an alteration of the deltoid's lever arm.\n\nThe aim of the study is to investigate the impact of lateralization on functional outcome and deltoid EMG activity in comparison to a standard implantation technique.",[28,29,30],"Cuff Tear Arthropathy","Omarthrosis","Rotator Cuff Tear Arthropathy",[32,33,34,35,36],"reverse total shoulder arthroplasty","cuff tear arthropathy","lateralization","deltoid function","EMG","NOT_YET_RECRUITING","2026-05-02",{"date":40,"type":41},"2026-05-07","ACTUAL",{"date":43,"type":22},"2026-06",{"date":45,"type":22},"2027-12",{"name":47,"class":48},"Vienna Hospital Association","OTHER_GOV",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":23,"phases":60,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":49},"100473050","phase-4-bioinductive-patch-for-full-thickness-rotator-cuff-tears-100473050","NCT05439850","Bioinductive Patch for Full-Thickness Rotator Cuff Tears","Arthroscopic Rotator Cuff Repair Augmented With Bioinductive Implant for Full-Thickness Tears: A Randomized Controlled Study","Inclusion Criteria:\n\n* Indicated and scheduled for arthroscopic rotator cuff repair.\n* Full-thickness medium (1-3 cm), large (3-5 cm), and massive (\\>5 cm) rotator cuff tears involving the supraspinatus and\u002For infraspinatus tendons demonstrated on magnetic resonance or ultrasound imaging.\n* Chronic, degenerative rotator cuff tears.\n* Ability to read and understand English.\n* Age ≥18 years\n* Patient failed ≥6 weeks of conservative treatment, which included structured, in-person physical therapy or documented home therapy\n\nExclusion Criteria:\n\n* Patient scheduled for open or mini-open rotator cuff repair\n* Prior surgery of affected shoulder (except diagnostic arthroscopy)\n* Partial-thickness rotator cuff tears\n* Small (\\\u003C1 cm) rotator cuff tears\n* Rotator cuff tears involving the subscapularis tendon\n* Acute and traumatic rotator cuff tears\n* Active infection\n* Cancer\n* Autoimmune and rheumatologic disorders, including rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosus","18 Years",{"count":59,"type":22},78,[61],"PHASE4","The purpose of this randomized-controlled study is to compare outcomes of arthroscopic rotator cuff repair augmented with a Bioinductive Implant (study group) to standard arthroscopic rotator cuff repair (control group). The primary outcome of this study is rotator cuff repair integrity (absence of full- or partial-thickness defect) demonstrated on ultrasound at 1-year postoperatively. The investigators hypothesize that the study group will have higher rates of repair integrity demonstrated on ultrasound at 1-year postoperatively.",[64,30],"Rotator Cuff Tears",[66,67,68,30],"Rotator Cuff Tear","Bioinductive","Arthroscopic Rotator Cuff Repair","RECRUITING","2026-02-24",{"date":72,"type":41},"2026-02-27",{"date":74,"type":41},"2022-08-16",{"date":76,"type":22},"2029-07-01",{"name":78,"class":79},"Henry Ford Health System","OTHER",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":89,"phases":4,"briefSummary":90,"conditions":91,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":105},"100444447","perform-humeral-system-study-100444447","NCT05067543","Perform Humeral System Study","PHS","Inclusion Criteria:\n\n* 18 years or older at the time of the informed consent or non-opposition (when applicable).\n* Informed and willing to sign an informed consent form approved by IRB or EC (when applicable).\n* Willing and able to comply with the requirements of the study protocol.\n* Considered a candidate for shoulder arthroplasty using a study device.\n* Meets indications for use requirements or other local, regional, or geographic specific regulatory requirements\n\nExclusion Criteria:\n\n* Not able to comply with the study procedures based on the judgment of the assessor (e.g. cannot comprehend study questions, inability to keep scheduled assessment times)\n* Patient belongs to a vulnerable group of patients, including minor patients, those unable to decide for themselves to participate or needing a Legally Authorized Representative (LAR), or others who could be subject to coercion (patients who may not be acting on their own initiative) (referred as \"vulnerable subject\" in the section 3.44 of the ISO 14155 norm).\n* Active local or systemic infection, sepsis, or osteomyelitis\n* Poor bone quality, where there could be considerable migration of the prothesis and\u002For a chance of fracture of the humerus or glenoid\n* Significant injury to the brachial plexus\n* Inadequate bone stock in the proximal humerus or glenoid fossa for supporting the components\n* Neuromuscular disease (e.g., joint neuropathy)\n* Patient with known allergy to one of the product materials\n* Metabolic disorders which may impair bone formation\n* Patient pregnancy\n* Planned for two-stage surgery",{"count":88,"type":22},300,"OBSERVATIONAL","This study is an international, single arm, multicenter, prospective, non-significant risk, Post-Market Clinical Follow-up study, which is designed to collect safety and performance data at baseline, surgery, immediate post-op and annually through 10 years post-operation.\n\nData collected from this study will be used for purposes, including but not limited to, Post-Market Surveillance, peer-reviewed publications, education materials, regulatory submissions, and\u002For product development.",[92,93,94,30],"Osteoarthritis Shoulder","Avascular Necrosis","Post-traumatic Arthrosis of Other Joints, Shoulder Region","2026-02-19",{"date":97,"type":41},"2026-02-20",{"date":99,"type":41},"2021-09-12",{"date":101,"type":22},"2036-12-01",{"name":103,"class":104},"Stryker Trauma and Extremities","INDUSTRY",10,{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":11,"sex":17,"minAge":113,"maxAge":4,"enrollmentInfo":114,"targetDuration":4,"studyType":89,"phases":4,"briefSummary":116,"conditions":117,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":134},"100485642","exactech-shoulder-post-market-clinical-follow-up-study-100485642","NCT05603728","Exactech Shoulder Post Market Clinical Follow-up Study","An Open Label, Multi-Center, Retrospective and Prospective Evaluation of Shoulder Arthroplasty Clinical and Radiographic Outcomes","Inclusion Criteria:\n\n* Patient is indicated for shoulder arthroplasty (or has previously undergone shoulder arthroplasty)\n* Patient is skeletelly mature\n* Patient is expected to survive at least 2 years beyond surgery\n* Patient is willing to participate by complying with pre- and postoperative visit requirements\n* Patient is willing and able to read and sign a study informed consent form\n\nExclusion Criteria:\n\n* Osteomyelitis of the proximal humerus or scapula; if a systemic infection or a secondary remote infection is suspected or confirmed, implantation should be delayed until infection is resolved\n* Inadequate or malformed bone that precludes adequate support or fixation of the prosthesis\n* Medial humeral bone loss resulting in compromised humeral stem fixation\n* Proximal humeral bone loss extending distal to the surgical neck where there is compromised humeral stem fixation\n* Neuromuscular disorders that do not allow control of the joint\n* Significant injury to the brachial plexus\n* Non-functional deltoid muscles\n* Patient's age, weight, or activity level would cause the surgeon to expect early failure of the system\n* The patient is unwilling or unable to comply with the post-operative care instructions\n* Alcohol, drug, or other subtance abuse\n* Any disease state that could adversaly affect the function or longevity of the implant\n* Patient is pregnant\n* Patient is a prisoner\n* Patient is contraindicated for the surgery\n* Revision cases in which a stemmed humeral component was used (Stemless Shoulder System)\n* Metal allergy or sensitivity to the implants materials (Stemless Shoulder System)\n* Acute fracture of the proximal humerus and displacement of the tuberosities, displaced three or four part fractures of the proximal humerus (hemi-arthroplasty), or acture fracture of the proximal humerus with failure of the glenohumeral joint (total anatomic shoulder arthroplasty) (Stemless Shoulder System)\n* Acute fracture of the proximal humerus in combination with degenerative diseases of the glenohumeral joint and a grossly deficient, irreparable rotator cuff resulting in superior migration of the humeral head (reverse total shoulder arthroplasty) (Stemless Shoulder System)","21 Years",{"count":115,"type":22},20000,"The 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.",[118,119,64,30,120,121,122,123,124],"Osteo Arthritis Shoulders","Osteonecrosis","Ankylosing Spondylitis","Post-traumatic Osteoarthritis","Rheumatoid Arthritis","Fracture","Infections","2025-12-09",{"date":127,"type":41},"2025-12-15",{"date":129,"type":41},"2007-07-19",{"date":131,"type":22},"2031-12-31",{"name":133,"class":104},"Exactech",38,{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":11,"sex":17,"minAge":142,"maxAge":4,"enrollmentInfo":143,"targetDuration":4,"studyType":23,"phases":145,"briefSummary":146,"conditions":147,"keywords":149,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":151,"lastUpdatePostDateStruct":152,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":158,"locationsCount":49},"100612588","efficacy-and-safety-of-digital-therapeutics-for-improving-shoulder-function-after-rotator-cuff-repair-100612588","NCT07255534","Efficacy and Safety of Digital Therapeutics for Improving Shoulder Function After Rotator Cuff Repair","Efficacy and Safety of Digital Therapeutics for Improving Shoulder Function After Rotator Cuff Repair: A Prospective, Randomized, Parallel-Group, Evaluator-Blinded Study","Inclusion Criteria:\n\n1. Be an adult aged 19 or older.\n2. Have a diagnosis corresponding to Korean Standard Classification of Diseases codes M75.1 (rotator cuff tear) or S46.08 (other specified injuries of tendons and muscles at shoulder and upper arm), and have undergone rotator cuff repair (RCR) surgery, or RCR combined with procedures such as acromioplasty, biceps tenotomy, fixation, or labrum repair.\n3. Own a smartphone operating on the Android or iOS platform.\n4. Have received a full explanation of this clinical trial, understood it, voluntarily agreed to participate, and provided written consent to comply with study precautions.\n\nExclusion Criteria:\n\n1. History of previous rotator cuff repair surgery on the same site (revision surgery).\n2. Planning or recommendation by medical staff for contralateral rotator cuff repair surgery within one year after enrollment.\n3. Plans to receive direct manual therapy or invasive procedures (e.g., oriental medicine treatments, injections, regenerative therapies) at the surgical site through inpatient or outpatient care at another hospital within one year post-discharge.\n4. Presence of severe underlying conditions, neuromusculoskeletal disorders, visual impairment, uncontrolled diabetes, cardiovascular disorders, or other comorbidities that hinder participation in rehabilitation exercises.\n5. Difficulty using clinical trial medical devices due to cognitive impairment (e.g., dementia), visual impairment, or digital illiteracy.\n6. Other cases where the medical staff judges that unsupervised rehabilitation exercise is contraindicated or the principal investigator deems the subject unsuitable for the clinical trial.","19 Years",{"count":144,"type":22},70,[25],"1. Importance of Rehabilitation After Rotator Cuff Repair Rotator cuff tears are among the most common shoulder conditions in Korea. They can occur naturally with aging or result from trauma or overuse. When conservative treatments like medication or injections fail to relieve pain and restore function, rotator cuff repair surgery is necessary. Postoperative rehabilitation exercises are crucial for recovering shoulder function, reducing pain, and returning to daily activities. Many studies have emphasized the importance of staged rehabilitation and patient education after surgery, showing that active patient participation directly affects recovery. However, some patients rely on unverified internet sources (such as YouTube or online forums) or face limitations such as time, geographical constraints, or cost even when receiving face-to-face therapy.\n2. Advantages of Digital Therapeutics Digital therapeutic devices have emerged as a promising solution to these challenges. These smartphone applications deliver exercise and educational content tailored to postoperative rehabilitation, aiming to improve the disease state. They offer anytime, anywhere access without time or location restrictions and provide evidence-based, systematic, and personalized rehabilitation programs. Comprehensive educational materials enhance patient understanding and promote self-management skills, potentially increasing rehabilitation adherence.\n3. Recent Research Findings Digital rehabilitation programs for patients after rotator cuff repair have demonstrated effectiveness. Programs that provide real-time exercise feedback using mobile apps and sensors have shown similar or superior outcomes compared to traditional physical therapy. Augmented reality (AR)-based rehab systems are more effective in improving shoulder function than conventional methods, and digital apps offering customized exercise videos significantly enhance physical function and confidence. Notably, patients using digital rehabilitation programs for 1 to 6 months exhibited improved adherence to therapeutic exercises, facilitating consistent home-based rehabilitation.\n4. Purpose of This Clinical Trial While previous studies have confirmed the efficacy and safety of digital therapeutic devices after rotator cuff surgery, most are limited to generic exercise programs. This clinical trial aims to evaluate the effectiveness and safety of a clinical trial digital therapeutic device not yet approved domestically, providing disease-specific exercise programs.",[30,148],"Repair of a Cuff Tear",[150],"Rotator Cuff Tear Arthropathy, repair of a cuff tear, digital therapeutics, rehabilitarion","2025-11-20",{"date":153,"type":41},"2025-12-01",{"date":155,"type":41},"2025-10-20",{"date":157,"type":22},"2026-12-31",{"name":159,"class":79},"Samsung Medical Center",{"id":161,"slug":162,"hasResults":11,"nctId":163,"briefTitle":164,"officialTitle":165,"acronym":4,"eligibilityCriteria":166,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":167,"targetDuration":4,"studyType":23,"phases":169,"briefSummary":170,"conditions":171,"keywords":174,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":179,"lastUpdatePostDateStruct":180,"startDateStruct":182,"completionDateStruct":184,"leadSponsor":186,"locationsCount":188},"100538540","pectoralis-minor-release-versus-non-release-in-rsa-100538540","NCT06292169","Pectoralis Minor Release Versus Non-release in RSA","A Randomized Control Trial to Evaluate Release Versus Non-release of Pectoralis Minor With Reverse Shoulder Arthroplasty","Inclusion Criteria:\n\n* All patients undergoing surgery for reverse total shoulder arthroplasty\n* Patients willing and able to provide informed consent\n\nExclusion Criteria:\n\n* Revision arthroplasty\n* Reverse shoulder arthroplasty for proximal humerus fractures\n* Adults unable to consent\n* Individuals who are not yet adults (infants, children, teenagers)\n* Pregnant women\n* Prisoners",{"count":168,"type":22},90,[25],"The goal of this clinical trial is to assess if concomitant open pectoralis minor release would improve pain and outcomes after Reverse Shoulder Arthroplasty (RSA). The main questions it aims to answer are:\n\n* whether releasing the pectoralis minor prophylactically could have better pain relief\n* whether releasing the pectoralis minor prophylactically could have increased Range of motion (ROM) outcomes\n* whether releasing the pectoralis minor prophylactically could have higher final Patient Reported Outcome Measurements (PROMs) Participants will be randomized to either undergo RSA with pectoralis minor release or RSA without pectoralis minor release.",[172,30,173],"Reverse Total Shoulder Arthroplasty","Advanced Glenohumeral Osteoarthritis",[172,175,176,177,178],"Reverse Shoulder Arthroplasty","American Shoulder and Elbow","Range of motion","Pectoralis Minor","2025-10-22",{"date":181,"type":41},"2025-10-23",{"date":183,"type":41},"2024-08-07",{"date":185,"type":22},"2026-01",{"name":187,"class":79},"Emory University",2,{"id":190,"slug":191,"hasResults":11,"nctId":192,"briefTitle":193,"officialTitle":194,"acronym":4,"eligibilityCriteria":195,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":196,"targetDuration":4,"studyType":89,"phases":4,"briefSummary":198,"conditions":199,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":205,"startDateStruct":207,"completionDateStruct":209,"leadSponsor":211,"locationsCount":49},"100510452","clinical-and-radiological-outcomes-of-medacta-shoulder-system-fr-100510452","NCT05926622","Clinical and Radiological Outcomes of Medacta Shoulder System FR","Clinical and Radiological Outcomes of Medacta Shoulder System","Inclusion Criteria:\n\n* Patients older than 18 years\n* Patient with one of the following diagnosis:\n\nPrimary osteoarthritis Secondary osteoarthritis Cuff tear arthropathy; insufficient rotator cuff Acute fracture (\\\u003C21d) Rheumatoid or inflammatory arthritis Avascular necrosis Other posttraumatic condition Revision of shoulder arthroplasty\n\nExclusion Criteria:\n\n* Patients with malignant diseases (at the time of surgery)\n* Patients with proven or suspect infections (at the time of surgery)\n* Patients with functional deficits other than dysfunction of the shoulder (at the time of surgery)\n* Patients with known incompatibility or allergy to products materials (at the time of surgery)",{"count":197,"type":22},200,"This is a post-marketing surveillance on Medacta Shoulder System",[200,201,30,202,93,123,203],"Primary Osteoarthritis","Secondary Osteoarthritis","Rheumatoid Arthritis Shoulder","Revision of Shoulder Arthroplasty","2025-09-23",{"date":206,"type":41},"2025-09-29",{"date":208,"type":41},"2022-03-15",{"date":210,"type":22},"2037-03",{"name":212,"class":104},"Medacta International SA",{"id":214,"slug":215,"hasResults":11,"nctId":216,"briefTitle":217,"officialTitle":217,"acronym":4,"eligibilityCriteria":218,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":219,"enrollmentInfo":220,"targetDuration":222,"studyType":89,"phases":4,"briefSummary":223,"conditions":224,"keywords":226,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":230,"lastUpdatePostDateStruct":231,"startDateStruct":233,"completionDateStruct":235,"leadSponsor":237,"locationsCount":49},"100565634","from-rotator-cuff-repair-to-reverse-shoulder-arthroplasty---clinical-and-radiological-results-100565634","NCT06644729","From Rotator Cuff Repair to Reverse Shoulder Arthroplasty - Clinical and Radiological Results","Inclusion Criteria:\n\n* Operated at Lovisenberg Diaconal Hospital in the time period 2010-2014 with an arthroscopic rotator cuff repair\n* Included in the rotator cuff registry at Lovisenberg Diaconal Hospital\n* Able to read and write Norwegian\n\nExclusion Criteria:\n\n* Lack of competence to consent\n* Not able to submit patient reported outcome measurements in any way and not able to undergo x-ray\n* Patient is unwilling to participate","95 Years",{"count":221,"type":22},733,"10 Years","In the planned study the investigators will invite 733 participants 10 years after arthroscopic rotator cuff repair to a follow up examination.\n\nShoulder pain is a common problem in the Norwegian population. Rotator cuff tear is a major cause of shoulder pain with a reported prevalence of up to 51% in patients 60-80 years of age. Arthroscopic rotator cuff repair is performed in an increasing proportion of these patients. Good results in shoulder function has been reported, although there is a lack in published good quality studies and long term follow up of these patients. There is also a lack of evidence regarding the association between radiologically-verified re-tear and clinical outcome.\n\nIn this project, the investigators address these critical gaps in knowledge and aim to investigate the factors influencing the clinical outcome after rotator cuff surgery and re-tear in a large prospective cohort study. The investigators will investigate how many participants suffering from poor outcome and develop cuff arthropathy in need of reverse shoulder arthroplasty after 10 years.",[64,30,225],"Rotator Cuff Injuries",[227,228,66,229],"PROM","Rotator Cuff Repair","Cuff Arthropathy","2024-10-18",{"date":232,"type":41},"2024-10-22",{"date":234,"type":41},"2024-09-11",{"date":236,"type":22},"2025-12",{"name":238,"class":79},"Lovisenberg Diakonale Hospital",{"id":240,"slug":241,"hasResults":11,"nctId":242,"briefTitle":243,"officialTitle":244,"acronym":245,"eligibilityCriteria":246,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":247,"targetDuration":4,"studyType":89,"phases":4,"briefSummary":249,"conditions":250,"keywords":251,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":253,"lastUpdatePostDateStruct":254,"startDateStruct":256,"completionDateStruct":258,"leadSponsor":260,"locationsCount":49},"100403169","clinical-study-evaluating-outcomes-of-reverse-shoulder-arthroplasty-with-smr-stemless-100403169","NCT04529798","Clinical Study Evaluating Outcomes of Reverse Shoulder Arthroplasty With SMR Stemless","A Monocentric Clinical Study Evaluating Clinical and Patient-reported Outcomes of Reverse Shoulder Arthroplasty With SMR Stemless","SSPR","Inclusion Criteria:\n\n* rotator-cuff arthropathy, osteoarthritis\n* approving written informed consent\n\nExclusion Criteria:\n\n* Female patients who are pregnant, nursing, or planning a pregnancy.\n* All adult patients with any of the SMR Stemless contraindication for use for the reverse configuration as reported in the current local Instruction for use.\n* not consenting in participating in this study",{"count":248,"type":22},60,"The objectives of this study are the assessment of the clinical, radiographical and patient-reported outcomes of SMR Stemless Reverse Shoulder Arthroplasty (LimaCorporate S.p.A.) used as standard of care over a period of at least 2 years of follow-up and the evaluation of the incidence of any complication.",[30,118],[252],"stemless reverse shoulder arthroplasty","2024-07-30",{"date":255,"type":41},"2024-07-31",{"date":257,"type":41},"2016-11-22",{"date":259,"type":22},"2025-08-30",{"name":261,"class":79},"Arthro Medics AG"]