[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"arthroplasty-replacement-shoulder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:arthroplasty-replacement-shoulder":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,69,96],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100401451","phase-4-intravenous-dexamethasone-administration-in-patients-undergoing-total-shoulder-arthroplasty-100401451",false,"NCT04507412","Intravenous Dexamethasone Administration in Patients Undergoing Total Shoulder Arthroplasty","Effect of Perioperative Intravenous Dexamethasone Administration in Patients Undergoing Total Shoulder Arthroplasty for Osteoarthritis, in Terms of Post-operative Pain, Function, Nausea, Hospitalization Length, and Risk of Complications","Inclusion Criteria:\n\n* Patients undergoing unilateral primary total anatomical or reverse shoulder arthroplasty (Total Shoulder Arthroplasty)\n* Patients with a BMI \\>18.5 and \\\u003C35\n* Patients able to provide informed consent and follow all the study procedures as indicated by the protocol\n* Informed Consent as documented by signature\n\nExclusion Criteria:\n\n* Contraindications to steroids\n* Revision and post-traumatic TSA\n* Active steroid or immunosuppressive therapy in the last 30 days before the operation\n* Pregnant or breast-feeding women\n* Presence of other clinically significant concomitant disease states (ASA IV)\n* Uncontrolled diabetes mellitus\n* Contraindications to Non-steroidal anti-inflammatory drugs\n* Chronic systemic diseases as immunodeficiency, autoimmune disease (Systemic Lupus Erythematosus), gout, rheumatic arthritis\n* Known or suspected non-compliance, drug or alcohol abuse\n* Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant.\n* Participation in another study with investigational drug within the 30 days preceding and during the present study\n* Previous enrolment into the current study\n* Enrolment of the investigator, his\u002Fher family members, employees and other dependent persons","ALL","58 Years","85 Years",{"count":20,"type":21},74,"ESTIMATED","INTERVENTIONAL",[24],"PHASE4","The aim of the study is to evaluate if intravenous steroid supplementation can provide advantages over routine analgesia protocols in terms of post-operative symptoms (pain and nausea), length of hospital stay, shoulder range of motion, function and patient satisfaction",[27],"Arthroplasty, Replacement, Shoulder",[29,30],"Total Shoulder Arthroplasty","steroid","RECRUITING","2026-03-03",{"date":34,"type":35},"2026-03-05","ACTUAL",{"date":37,"type":35},"2020-09-09",{"date":39,"type":21},"2032-08-31",{"name":41,"class":42},"Christian Candrian","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":43},"100584594","at-home-digital-rehabilitation-for-patients-after-reverse-total-shoulder-arthroplasty-100584594","NCT06891378","At Home, Digital Rehabilitation for Patients After Reverse Total Shoulder Arthroplasty","Effects of Mobile App-based Self-rehabilitation for Patients After Reverse Total Shoulder Arthroplasty: Pilot Non-RCT","DHI_RTSA","Inclusion criteria\n\n* Those aged 50 or older\n* Those who are indicated for and are scheduled to undergo reverse total shoulder arthroplasty (RTSA)\n* Those who voluntarily decided to participate and gave written consent after hearing a detailed explanation of this study\n\nExclusion criteria\n\n* Those who have difficulty using the application due to severe underlying diseases, neuromusculoskeletal diseases, cognitive or visual impairments, etc.\n* Those with concomitant diseases such as neurological or visual impairments or uncontrolled cardiovascular disorders that make it difficult to participate in rehabilitation exercises\n* Other people who, as determined by a medical professional, should not perform rehabilitation exercises without supervision","50 Years",{"count":54,"type":21},100,[56],"NA","1. Why This Study Matters Over the past five years, more people in Korea have been having shoulder surgery. With our country moving into a super-aged society by 2025, these surgeries are expected to increase even more. More people today are focused on staying healthy and active, so many are choosing shoulder surgery to enjoy a better quality of life. According to the Health Insurance Review and Assessment Service, around 90,000 shoulder surgeries take place each year, and most of these patients (84.6%) are over 50.\n2. Reverse Shoulder Arthroplasty (RTSA) and the Role of Rehabilitation RTSA is a type of shoulder surgery often used when there's extensive damage to the shoulder's rotator cuff. Its use is growing rapidly-making up about one-third of shoulder replacements in the United States and over 90% in some European countries. Although shoulder replacement surgeries are increasing worldwide, we still need more research on the best ways to help patients recover. In particular, we want to see if using a mobile app for self-guided rehabilitation can be effective.\n3. The Need for Mobile App-Based Self-Rehabilitation After shoulder surgery, proper rehabilitation is crucial for a good recovery. Recent studies have shown that a mobile app can help patients easily follow their rehabilitation exercises. It also improves their understanding of the recovery process and keeps them more engaged in their treatment. Previous research has even shown that patients recovering from knee or hip replacement surgeries experienced better physical and mental recovery when using a mobile app.\n4. Benefits of Using Technology for Rehabilitation Studies have found that patients who use remote rehabilitation techniques gain more confidence in managing their recovery on their own rather than relying solely on regular hospital visits. In one small study, five patients who used remote rehabilitation after RTSA reported high satisfaction with their recovery process. Mobile apps also allow healthcare providers to check that patients are doing their exercises correctly and to offer timely advice. This improved communication helps patients be more proactive about their recovery.\n5. What This Study Aims to Do\n\nThis study will explore how mobile app-based self-rehabilitation affects recovery after shoulder replacement surgery. We will compare two groups of patients:\n\nOne group will use a mobile app to guide their rehabilitation. The other group will follow traditional rehabilitation instructions provided in a brochure.",[27,59],"Reverse Total Shoulder Arthroplasty","2025-06-23",{"date":62,"type":35},"2025-06-26",{"date":64,"type":35},"2025-06-20",{"date":66,"type":21},"2026-06-30",{"name":68,"class":42},"Samsung Medical Center",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":16,"minAge":76,"maxAge":77,"enrollmentInfo":78,"targetDuration":4,"studyType":80,"phases":4,"briefSummary":81,"conditions":82,"keywords":83,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":43},"100441580","testosterone-levels-and-cutibacterium-100441580","NCT05030220","Testosterone Levels and Cutibacterium","Association Between Serum Testosterone Levels and Cutibacterium Culture Positivity During Shoulder Arthroplasty","Phase 1 Inclusion Criteria:\n\n* Patients having elective shoulder arthroplasty\n\nPhase 1 Exclusion Criteria:\n\n* history of shoulder septic arthritis\n* antibiotic use within 3 months prior to surgery\n* recent treatment for acne\n* Lacked fluency in English\n\nPhase 2 Inclusion Criteria:\n\n* Patients having elective shoulder arthroplasty\n\nPhase 2 Exclusion Criteria:\n\n* Lacked fluency in English","18 Years","89 Years",{"count":79,"type":21},300,"OBSERVATIONAL","Phase 1: In 51 patients undergoing shoulder arthroplasties, total serum testosterone, free testosterone and sex hormone binding globulin levels obtained in the clinic before surgery were correlated with the levels of Cutibacterium on the skin in clinic, in the operating room prior to surgery, and in the skin incision.\n\nPhase 2: The investigators wish to determine if preoperative serum testosterone levels are associated with risk for shoulder PJI (periprosthetic joint infection) in patients undergoing primary shoulder arthroplasty. Also to determine if preoperative serum testosterone levels are predictive of bacterial load of deep tissue cultures taken at the time of revision shoulder arthroplasty in patients undergoing primary shoulder arthroplasty.",[27],[84,85,86],"Testosterone","Cutibacterium","Shoulder Arthroplasty","2025-03-25",{"date":89,"type":35},"2025-03-30",{"date":91,"type":35},"2020-07-01",{"date":93,"type":21},"2027-01-01",{"name":95,"class":42},"University of Washington",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":102,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":16,"minAge":104,"maxAge":105,"enrollmentInfo":106,"targetDuration":4,"studyType":22,"phases":108,"briefSummary":109,"conditions":110,"keywords":112,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":125},"100518037","does-bio-rsa-provides-superior-clinical-outcome-compared-to-conventional-rsa-100518037","NCT06025331","Does BIO-RSA Provides Superior Clinical Outcome Compared to Conventional RSA?","From Cuff Arthropathy to Reverse Shoulder Arthroplasty - a Multicentre Randomized Control Trial (Study 1: Does BIO-RSA Provides Superior Clinical Outcome Compared to Conventional RSA?).","CARS-1","Inclusion Criteria:\n\n* Eligible for primary RSA due to OA, massive RC tear, failed RC repair or post-instability osteoarthritis\n* Able to read or write Norwegian\n\nExclusion Criteria:\n\n* Severe osteoporosis\n* Osteonecrosis of the humeral head\n* Dementia\n* Poor deltoid function\n* Revision surgery\n* ASA IV\n* Suspected chronic infection\n* Acute fracture","45 Years","80 Years",{"count":107,"type":21},130,[56],"The goal of this clinical trial is to compare two different types of reverse shoulder replacements. Researchers will compare a conventional reverse shoulder replacement with a lateralized reverse shoulder replacement to see if there is a difference in how well the patients function after two years.",[27,111],"Shoulder Osteoarthritis",[113,114,115],"Reverse Shoulder Arthroplasty","BIO-RSA","Orthopedic surgery","2023-11-06",{"date":118,"type":35},"2023-11-07",{"date":120,"type":35},"2023-09-15",{"date":122,"type":21},"2033-08-01",{"name":124,"class":42},"Lovisenberg Diakonale Hospital",2]