[{"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":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"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":4,"briefSummary":22,"conditions":23,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100226855","observational-study-to-evaluate-long-term-outcome-in-hip-arthroplasty-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":19,"type":20},2500,"ESTIMATED","OBSERVATIONAL","This long-term outcomes study is designed to collect safety and efficacy data on designated, commercially available, hip arthroplasty products.",[24,25,26,27,28],"Hip Replacement","Primary, Secondary or Post-traumatic Osteoarthrosis","Femur Head Necrosis","Congenital Dislocations","Primary and Revision Surgery",[30,24,31,32],"Arthroplasty","Acetabular cup","Femoral stem","RECRUITING","2026-03-17",{"date":36,"type":37},"2026-03-18","ACTUAL",{"date":39,"type":4},"2014-05",{"date":41,"type":20},"2044-12",{"name":43,"class":44},"Corin","INDUSTRY",13,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":66},"100529345","spartan-stem-world-cup-and-world-liner-post-market-clinical-follow-up-study-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":54,"type":20},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.",[24],"2023-12-07",{"date":59,"type":37},"2023-12-15",{"date":61,"type":20},"2023-12-08",{"date":63,"type":20},"2028-04-01",{"name":65,"class":44},"Signature Orthopaedics",1]