[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Corin\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":72},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"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":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100491987","observational-study-to-evaluate-long-term-outcome-in-hip-hemiarthroplasty-100491987",false,"NCT05686278","Observational Study to Evaluate Long-Term Outcome in Hip Hemiarthroplasty","A Post-market Clinical Follow-up (PMCF) Study to Evaluate Clinical, Radiographic and Patient Reported Outcomes Following a Hip Hemiarthroplasty Surgery Using Corin Devices","Inclusion Criteria:\n\n1. Both genders.\n2. Adult subjects.\n3. Subjects clinically suitable for a hip hemiarthroplasty surgery with Corin hip devices based on physical examination, medical history and diagnosis such as: non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis in which the acetabulum does not require replacement, treatment of non-union, femoral neck and trochanteric fractures of the proximal femur, revision of failed partial hip replacements in which the acetabulum does not require replacement.\n4. The subject is willing to comply with the required follow-up visits as per protocol.\n5. The subject, or a designated trusted person in case the subject is unable to do, has signed a Patient Informed Consent Form (PICF), specific to this study, and approved by the local EC.\n\nExclusion Criteria:\n\n1. Subjects with active infection or sepsis or osteomyelitis.\n2. Subjects with unsuitable or insufficient bone support preventing proper fixation of the prosthesis.\n3. Subject with marked bone loss or bone absorption.\n4. Subject with metabolic disorders which may impair bone formation or bone quality.\n5. Subjects under guardianship.\n6. Subjects under jusicial protection\n7. Subjects in the opinion of the Investigator\u002F investigative team who will be unable to comply with study procedures (Examples: recent psychotic or mania disorders, alcohol, drug or substance abusers) and\u002For those unable for any medical or other reason to comply with study procedures\u002Fvisits.","ALL","18 Years",{"count":19,"type":20},368,"ESTIMATED","OBSERVATIONAL","This PMCF study is designed to collect safety and efficacy data on hip hemiarthroplasty surgeries with Corin BiPolar-i shell and the Oceane+ or Meije Duo femoral stem up to 10 years.",[24,25,26,27,28],"Hip Fractures","Hip Hemiarthroplasty","Osteoarthritis, Hip","Avascular Necrosis of Hip","Femoral Neck Fractures",[30,31,24],"Hemiarthroplasty","Acetabulum","RECRUITING","2026-03-17",{"date":35,"type":36},"2026-03-18","ACTUAL",{"date":38,"type":36},"2023-06-29",{"date":40,"type":20},"2035-09",{"name":42,"class":43},"Corin","INDUSTRY",4,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":54,"conditions":55,"keywords":61,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":65,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},"100226855","observational-study-to-evaluate-long-term-outcome-in-hip-arthroplasty-100226855","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",{"count":53,"type":20},2500,"This long-term outcomes study is designed to collect safety and efficacy data on designated, commercially available, hip arthroplasty products.",[56,57,58,59,60],"Hip Replacement","Primary, Secondary or Post-traumatic Osteoarthrosis","Femur Head Necrosis","Congenital Dislocations","Primary and Revision Surgery",[62,56,63,64],"Arthroplasty","Acetabular cup","Femoral stem",{"date":35,"type":36},{"date":67,"type":4},"2014-05",{"date":69,"type":20},"2044-12",{"name":42,"class":43},13,""]