[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hip-replacement\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hip-replacement":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100226855",false,"NCT02230826","Observational Study to Evaluate Long-Term Outcome in Hip Arthroplasty","Multicentric Observational PMCF Study to Evaluate Long-term Outcome, Performance and Safety of Implantable Devices in Hip Arthroplasty","Inclusion Criteria:\n\n* Man or woman \\>18 years\n* Subjects with indication of arthroplasty surgery with Corin hip devices which are under assessment as part of this PMCF study\n* Subjects who agreed for study participation.\n\nExclusion Criteria:\n\n* Subjects with existing tumour and\u002For particularly high surgical risk-\n* Subjects with anaesthetic risk class IV or higher\n* Subjects under guardianship and\u002For unable to follow procedures or matters related to the study (examples: Illiterate, recent psychotic or mania disorders and \u002F or inability to comply with usual follow-up visits.)\n* Contraindications for arthroplasty with a Corin hip devices as per product IFU","ALL","18 Years",{"count":18,"type":19},2500,"ESTIMATED","OBSERVATIONAL","This long-term outcomes study is designed to collect safety and efficacy data on designated, commercially available, hip arthroplasty products.",[23,24,25,26,27],"Hip Replacement","Primary, Secondary or Post-traumatic Osteoarthrosis","Femur Head Necrosis","Congenital Dislocations","Primary and Revision Surgery",[29,23,30,31],"Arthroplasty","Acetabular cup","Femoral stem","RECRUITING","2026-03-17",{"date":35,"type":36},"2026-03-18","ACTUAL",{"date":38,"type":4},"2014-05",{"date":40,"type":19},"2044-12",{"name":42,"class":43},"Corin","INDUSTRY",13,{"id":46,"slug":4,"hasResults":10,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":64},"100529345","NCT06172569","Spartan Stem, World Cup and World Liner Post Market Clinical Follow-up Study","Inclusion Criteria:\n\n* patient requires unilateral primary total hip arthroplasty due to non-inflammatory degenerative joint disease (e.g., osteoarthritis, traumatic arthritis, avascular necrosis, dysplasia\u002FDDH)\n* patient must be a candidate for use of the products studied, as determined jointly by the surgeon and patient.\n* male and non-pregnant female patients aged 18-75\n* patients who understand the conditions of the clinical evaluation and are willing to participate for the length of the prescribed follow-up.\n\nExclusion Criteria:\n\n* patient has active infection or sepsis(treated or untreated) enough to compromise implant stability or postoperative recovery\n* patient is a female of child-bearing age and not taking and not taking contraceptive pills\n* patient has inadequate bone stock to support the device (e.g. severe osteopenia, family history of severe osteoporosis or osteopenia)\n* patient has a known or suspected metal sensitivity\n* patient is immuno-suppressed with disease such as AIDS or is receiving high dose of cortico-steroids.\n* patient has an emotional or neurological condition that would pre-empt their ability or unwillingness to participate in the clinical evaluation including mental illness, mental retardation or drug abuse\n* patient is severely overweight with a BMI\\>40.","75 Years",{"count":52,"type":19},200,"The aim of the study is to monitor the performance of the Signature Orthopaedics Spartan Stem, World Acetabular Cup and World Liner as a post-market vigilance and continuous improvement efforts.",[23],"2023-12-07",{"date":57,"type":36},"2023-12-15",{"date":59,"type":19},"2023-12-08",{"date":61,"type":19},"2028-04-01",{"name":63,"class":43},"Signature Orthopaedics",1,""]