[{"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":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,77],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100649404","sarcopenia-screening-in-advanced-coxarthrosis-the-sarco-cox-study-100649404",false,"NCT07734129","Sarcopenia Screening in Advanced Coxarthrosis: The SARCO-COX Study","Efficacy of a Sarcopenia Screening Program in Subjects With Advanced Coxarthrosis. SARCO-COX Randomized Intervention Study","SARCO-COX","Inclusion Criteria:\n\n* Subjects age \\>= 65 years of age\n* Previous diagnosis of advanced hip osteoarthritis.\n* Patients who are on the surgical waiting list for total joint replacement hip.\n* Barthel Index \\> 80 points.\n* That they will undergo surgery at the Regional University Hospital of Malaga.\n\nExclusion Criteria:\n\n* Patients who refuse to accept and sign the informed consent form surgical intervention.\n* Patients who refuse to accept and sign the informed consent form participation in the study.\n* Subjects diagnosed with immunodeficiency or undergoing immunosuppressive treatment.\n* Subjects diagnosed with inflammatory or hematological disease.\n* Subjects with coagulation disorders.\n* Subjects with lung disease, heart disease or unstable high blood pressure.\n* Subjects diagnosed with neurodegenerative disease that prevents them from performing physical exercise.\n* Subjects with psychiatric pathology that prevents the performance of physical exercise and adherence to treatment.","ALL","65 Years",{"count":20,"type":21},150,"ESTIMATED","INTERVENTIONAL",[24],"NA","The SARCO-COX study evaluates whether screening for sarcopenia (loss of muscle strength and mass) in adults aged 65 years or older with advanced hip osteoarthritis, followed by a structured postoperative exercise program, improves recovery after total hip replacement surgery compared with standard care.\n\nParticipants will undergo assessments of muscle strength, muscle mass, physical function, pain, and quality of life before surgery and during follow-up. Blood samples and a small muscle biopsy obtained during the planned surgery will be analyzed to study biomarkers related to muscle health.\n\nA total of 150 people are expected to participate in this study. Participants will be divided into three groups:\n\n* Group 1: People with sarcopenia who will take part in an exercise programme following surgery.\n* Group 2: People with sarcopenia who will receive the usual care and follow-up after their surgery.\n* Group 3: people without sarcopenia who are undergoing surgery and will receive the usual care and follow-up.\n\nThe study aims to determine whether early identification and targeted rehabilitation of sarcopenia can improve functional outcomes and quality of life after hip replacement.",[27,28],"Sarcopenia","Coxarthrosis",[30,31,32,27,33],"Muscle strength","Biomarkers","Exercise therapy","Hip arthrosis","NOT_YET_RECRUITING","2026-07-24",{"date":37,"type":38},"2026-07-29","ACTUAL",{"date":40,"type":21},"2026-07-01",{"date":42,"type":21},"2029-09-01",{"name":44,"class":45},"Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":61,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":46},"100537022","comparison-of-the-restoration-of-hip-biomechanical-parameters-by-ct-measurement-between-the-3-surgical-techniques-rsaminihiptha---hip-replacement-3d-planning-100537022","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.","18 Years",{"count":57,"type":21},165,"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",[28],[62,63,64,65,66],"Arthroplasty hip","femoral offset","resurfacing","EOS","3D","RECRUITING","2026-05-18",{"date":70,"type":38},"2026-05-19",{"date":72,"type":38},"2024-05-27",{"date":74,"type":21},"2026-08-27",{"name":76,"class":45},"University Hospital, Lille",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":86,"conditions":87,"keywords":88,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":46},"100608299","comparison-of-complication-rate-functional-outcome-and-quality-of-life-between-standard-therapy-versus-fast-track-therapy-in-patients-following-hip-replacement-surgery-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":85,"type":21},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.",[28],[89,90],"enhanced recovery","physiotherapy","2025-09-26",{"date":93,"type":38},"2025-09-30",{"date":95,"type":38},"2025-06-01",{"date":97,"type":21},"2025-12-31",{"name":99,"class":45},"Technical University of Munich"]