[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"coxarthrosis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:coxarthrosis":66},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100537022",false,"NCT06272422","Comparison of the Restoration of Hip Biomechanical Parameters by CT Measurement Between the 3 Surgical Techniques: RSA\u002FMinihip\u002FTHA - Hip Replacement: 3D Planning","Comparison of the Restoration of Hip Biomechanical Parameters by CT Measurement Between the 3 Surgical Techniques: RSA\u002FMinihip\u002FTHA","HIP3D","Inclusion Criteria:\n\n* Male or female\n* Age ≥ 18 years\n* Planned surgery: total hip arthroplasty, Minihip or RSA\n* Absence of osteoarthritis or osteoarthritis ≤ stage 1 (Tönnis classification) of contralateral hip (Radiographic analysis)\n* Patient having given his\u002Fher non-opposition to participate in the study\n* Patient with social insurance\n* Patient willing to comply with all study procedures and duration\n\nExclusion Criteria:\n\n* Patient with comorbidity(ies) likely to affect biomechanical parameter measurements or surgical conditions:\n* Anomalies or anatomical changes of the hip, pelvis or lumbar spine (history of fracture, protrusion, scoliosis, history of orthopedic surgery, dysplasia, torsion disorder)\n* Established genetic disease affecting the musculoskeletal system\n* Severe or morbid obesity\n* Neuromuscular pathologies affecting the limb girdles\n* Severe osteoporosis\n* Bone location of primary or metastatic cancer (spine, pelvis or femur) - Inequality of lower limb length \\> 2 cm.\n* Minors\n* Protected adults\n* Pregnant or breast-feeding women\n* Administrative reasons: inability to receive informed information, inability to participate in the entire study, lack of social security coverage, refusal to participate.","ALL","18 Years",{"count":19,"type":20},165,"ESTIMATED","OBSERVATIONAL","The study will analyze hip biomechanical parameters using EOS radiographic measurements pre- and post-operatively (3 months) and post-operatively (3 months) CT scans after total hip replacement (THR), neck-preserving THR of the Minihip type or hip resurfacing (HR). Clinical results will be assessed at 3 months and 1 year after surgery.\n\nTo this end, two types of examination are carried out, both of which are used in current practice:\n\n* Pre-operatively: EOS radiography\n* Post-operatively: EOS radiograph and CT scan\n\nInclusion (m-3; m-1) :\n\n* Patient information at pre-operative visit\n* Non-opposition of patient, family member or legal guardian, if applicable\n* Questionnaires and clinical examination (standard management)\n* EOS during anesthetic consultation\n\nFollow-up visit (m+3):\n\n\\- Post-operative follow-up consultation EOS and CT scan (1 week prior to visit) + questionnaire and clinical examination\n\nFollow-up visit (m+12):\n\n\\- Post-operative check-up, questionnaire and clinical examination",[24],"Coxarthrosis",[26,27,28,29,30],"Arthroplasty hip","femoral offset","resurfacing","EOS","3D","RECRUITING","2026-05-18",{"date":34,"type":35},"2026-05-19","ACTUAL",{"date":37,"type":35},"2024-05-27",{"date":39,"type":20},"2026-08-27",{"name":41,"class":42},"University Hospital, Lille","OTHER",1,{"id":45,"slug":4,"hasResults":10,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":52,"conditions":53,"keywords":54,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":43},"100608299","NCT07199751","Comparison of Complication Rate, Functional Outcome and Quality of Life Between Standard Therapy Versus Fast-track Therapy in Patients Following Hip Replacement Surgery","Vergleich Der Komplikationsrate, Des Funktionellen Outcomes Und Der Lebensqualität Zwischen Standard Therapie Versus Fast Track Therapie Bei Patienten Und Patientinnen Nach Hüft-TEP Operationen","Inclusion Criteria:\n\n* Age ≥18 years\n* The patient will undergo surgery at Klinikum rechts der Isar, Technical University of Munich (TUM)\n* Written informed consent for participation in the study after detailed explanation of the nature, significance, risks and scope of the clinical trial\n* Written informed consent from the patient for data collection and data processing, with the patient fully informed.\n* Sufficient German language skills of the patient.\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years\n* The patient is under guardianship, legally incapacitated or has limited legal capacity\n* Only partial weight-bearing permitted",{"count":51,"type":20},90,"The fast track group vs. control group will be compared with regard to hospitalization time and the non-inferiority of the fast track group vs. control group with regard to HOOS will be assessed.\n\nThe questionnaires will only be collected in the study: Eq-5d-5l, HOOS, self-efficacy, enjoyment of movement, fear of movement, pain catastrophizing.",[24],[55,56],"enhanced recovery","physiotherapy","2025-09-26",{"date":59,"type":35},"2025-09-30",{"date":61,"type":35},"2025-06-01",{"date":63,"type":20},"2025-12-31",{"name":65,"class":42},"Technical University of Munich",""]