[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Waldemar Link GmbH & Co. KG\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":63},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":27,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":5},"100415358","clinical-and-functional-outcome-of-the-mobilelink-acetabular-cup-system-in-the-short--mid--and-longterm-follow-up-100415358",false,"NCT04688593","Clinical and Functional Outcome of the MobileLink Acetabular Cup System in the Short-, Mid-, and Longterm Follow-up","Inclusion Criteria:\n\n* Implantation of a MobileLink acetabular cup system and a femoral stem manufactured by Waldemar Link\n* Age ≥ 18 years\n* Fully signed patient informed cons\n\nExclusion Criteria:\n\n* Revisions\n* Body Mass Index (BMI) ≥ 40 kg\u002Fm²\n* Patient who is foreseeable not able to understand the study and the study-related circumstances\n* Patients who is foreseeable non-compliant to the treatment and the follow-ups\n* Pregnant or breast-feeding women\n* Prisoner","ALL","18 Years",{"count":18,"type":19},520,"ESTIMATED","OBSERVATIONAL","The implantation of artificial hip joints is one of the most frequently performed surgeries. Normally, patients are very satisfied with the results.\n\nThe MobileLink hip prosthesis system is a CE marked medical device. This means the the safety and performance of the prosthesis ist approved. Aim of the study is to collect clinical data about the outcome of the MobileLink hip prosthesis system under routine condition and to determine the satisfaction of the patients.",[23,24,25,26],"Osteoarthritis, Hip","Hip Osteoarthritis","Prosthesis Survival","Prosthesis Failure",[28],"MobileLink","RECRUITING","2024-01-24",{"date":32,"type":33},"2024-01-25","ACTUAL",{"date":35,"type":33},"2021-05-04",{"date":37,"type":19},"2036-01",{"name":39,"class":40},"Waldemar Link GmbH & Co. KG","INDUSTRY",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":51,"conditions":52,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":62},"100428385","clinical-and-functional-outcome-of-the-gemini-sl-fixed-bearing-ps-knee-prosthesis-100428385","NCT04858347","Clinical and Functional Outcome of the GEMINI SL Fixed Bearing PS Knee Prosthesis","Clinical and Functional Outcome of the GEMINI SL Fixed Bearing PS Knee Prosthesis in Short-, Mid-, and Longterm Follow-up","Inclusion Criteria:\n\n* Signed patient informed consent\n* Implantation of a GEMINI SL Fixed Bearing PS knee prosthesis\n* Age between 18 and 80 years\n\nExclusion Criteria:\n\n* Body Mass Index (BMI) \\> 40 kg\u002Fm²\n* Foreseeable life expectancy under 5 years\n* Comorbidities and known medical circumstances which would affect the clinical or functional outcome after implantation of the knee prosthesis (e.g. neurological or musculoskeletal diseases) at the time of implantation\n* Patient who is mentally not able to understand the study and the study conduct\n* Patients who will be foreseeable non-compliant to the planned routine interventions and study related follow-ups\n* Prisoner\n* Pregnant women","80 Years",{"count":50,"type":19},350,"This is a prospective, multicenter, observational study with a planned follow-up period of 10 years to confirm the safety and performance of the GEMINI SL Fixed Bearing PS knee prosthesis in longterm follow-up under routine conditions. Primary outcome of the study is the 10-year survival rate of the GEMINI SL Fixed Bearing PS knee prosthesis with revision for any reason as the endpoint.",[53],"Osteoarthrosis of Knee","2023-01-11",{"date":56,"type":33},"2023-01-12",{"date":58,"type":33},"2019-07-04",{"date":60,"type":19},"2035-10",{"name":39,"class":40},1,""]