[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"post-traumatic-arthrosis-of-other-joints-upper-arm\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:post-traumatic-arthrosis-of-other-joints-upper-arm":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100444040","mirror-medacta-shoulder-system-pivotal-trial-100444040",false,"NCT05062252","Mirror Medacta Shoulder System Pivotal Trial","Multicentric, Prospective, Comparative Trial to Assess the Efficacy and Safety of an Anatomic Total Shoulder System.","Inclusion Criteria:\n\n* Age ≥ 18 yr\n* Clinical indication for anatomic primary total shoulder replacement due to osteoarthritis and\u002For posttraumatic arthritis\n* Willingness and ability to comply with study protocol\n\nExclusion Criteria:\n\n* Medical condition or balance impairment that could lead to falls\n* Prior rotator cuff surgery\n* Cuff tear arthropathy\u002Finsufficient rotator cuff\n* Insufficient bone quality which may affect the stability of the implant\n* Neuromuscular compromise of shoulder or other disabilities affecting the maximum functional outcomes\n* Weight bearing shoulder due to wheel chair, crutches, rollator at the time of operation\n* Active metastatic or neoplastic disease at the shoulder joint\n* Chemotherapy treatment\u002Fradiotherapy within 6 mo before surgery\n* \\>5 mg\u002Fday of corticosteroids, excluding inhalers, within 3 years before surgery\n* Pregnancy or plan to become pregnant during study period\n* Inability to understand study or a history of noncompliance with medical advice\n* Alcohol or drug abuse\n* Current enrollment in any clinical research study that might interfere with this study\n* Metal allergies or sensitivity.\n* Previous or current infection at or near the site of implantation.\n* Current distant or systemic infection\n* Patient, whose infomed consent form should be taken in an emergency situation\n* ONLY for women of childbearing age: a positive pregnancy test (urine \u002F blood)","ALL","18 Years",{"count":19,"type":20},100,"ESTIMATED","INTERVENTIONAL",[23],"NA","The purpose of this study is to demonstrate safety and efficacy of the Mirror Medacta Shoulder System in total shoulder arthroplasty.",[26,27],"Arthritis Shoulder","Post-traumatic Arthrosis of Other Joints, Upper Arm","RECRUITING","2025-05-07",{"date":31,"type":32},"2025-05-08","ACTUAL",{"date":34,"type":32},"2022-01-05",{"date":36,"type":20},"2027-12-30",{"name":38,"class":39},"Medacta International SA","INDUSTRY",2]