[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dysplasia-of-hip-joint\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dysplasia-of-hip-joint":40},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":5},"100565329",false,"NCT06640764","Multicentre SMS Study - FR","Étude Prospective, Multicentrique, Non contrôlée, Non randomisée, Ouverte évaluant la Performance et la stabilité de l'Implant fémoral Non cimenté SMS","Inclusion Criteria:\n\n* Patient suffering from a severely painful and\u002For disabling hip joint due to osteoarthritis, traumatic arthritis, developmental dysplasia of the hip, or avascular necrosis of the femoral head, and requiring a total hip replacement.\n* Patient who will receive a Medacta SMS femoral stem.\n* Patient agrees to comply with the study requirements.\n* Patient has signed the consent form.\n* Patient is affiliated with a social security system.\n* Patient aged 18 to 75 years\n\nExclusion Criteria:\n\n* Participation in biomedical research.\n* Minor patient.\n* Protected adult patient.\n* Vulnerable individuals as defined by Article L1121-6 of the Public Health Code.\n* Pregnant or breastfeeding women.\n* Patient unable to express their non-opposition.\n* Patient refusing the collection of their personal data.\n* Acute, systemic, or chronic infection. Skeletal immaturity.\n* Grossly deformed anatomy (at the surgeon's discretion).\n* Osteomalacia for which the fixation of an uncemented implant is contraindicated.\n* Patient suffering from active rheumatoid arthritis or osteoporosis.\n* Patient with metabolic disorders likely to impair bone formation when the fixation of an uncemented implant is contraindicated.\n* Patient suffering from muscle atrophy or neuromuscular disease.\n* Patient with an allergy to the implant material.\n* Any patient who cannot or does not wish to give their informed consent to participate in the study.\n* Patient whose prospects of regaining independent mobility would be compromised by known coexisting medical problems.\n* Any contraindication mentioned in the instructions for use of the investigational medical device.","ALL","18 Years","85 Years",{"count":19,"type":20},260,"ESTIMATED","OBSERVATIONAL","Prospective, multicentre, non controled, non randomised, clinical study to assess the performance and the stability of SMS femoral stem",[24,25,26,27],"Dysplasia of Hip Joint","Hip Osteoarthritis","Traumatic Arthritis of Hip","Avascular Necrosis of Femur Head","RECRUITING","2024-10-11",{"date":31,"type":32},"2024-10-15","ACTUAL",{"date":34,"type":32},"2024-09-01",{"date":36,"type":20},"2037-09-01",{"name":38,"class":39},"Medacta International SA","INDUSTRY",""]