[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"developmental-dysplasia-of-the-hip-ddh\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:developmental-dysplasia-of-the-hip-ddh":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,53],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100637695","computer-assisted-comparison-of-hip-socket-volume-and-surface-shape-after-pediatric-acetabular-osteotomies-100637695",false,"NCT07581717","Computer-Assisted Comparison of Hip Socket Volume and Surface Shape After Pediatric Acetabular Osteotomies","Computer-Assisted Comparative Analysis of Acetabular Volume and Surface Morphology in Pediatric Acetabular Osteotomies (Salter, Dega, San Diego, and Pemberton)","PAVMS","Inclusion Criteria:\n\n1. Age 2 to 18 years\n2. Developmental dysplasia of the hip or residual acetabular dysplasia\n3. Primary Salter, Dega, San Diego, or Pemberton acetabular osteotomy planned at Istanbul University, Istanbul Faculty of Medicine\n4. Preoperative hip MRI available within 6 weeks before surgery\n5. Early postoperative hip MRI available 3 to 8 weeks after surgery\n6. MRI quality adequate for three-dimensional morphometric analysis\n7. Unilateral or bilateral cases eligible\n\nExclusion Criteria:\n\n1. Hip pathology not related to developmental dysplasia of the hip, including Perthes disease, slipped capital femoral epiphysis, neuromuscular dysplasia, or infection\u002Ftrauma sequelae\n2. Previous surgery on the same hip that significantly alters anatomy, including prior pelvic or femoral osteotomy or open reduction, or current metal implant\u002Ffusion\n3. MRI contraindication or safety issue, including MR-incompatible implant\u002Fdevice, severe claustrophobia, or a medical barrier to sedation\u002Fanesthesia\n4. MRI not compatible with protocol or inadequate for analysis","ALL","2 Years","18 Years",{"count":21,"type":22},12,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to learn how four acetabular osteotomy techniques change the shape of the hip socket in children and adolescents with developmental dysplasia of the hip or residual acetabular dysplasia.\n\nThe main questions it aims to answer are:\n\nHow do virtual Salter, Dega, San Diego, and Pemberton osteotomies differ in acetabular volume and surface shape on participant-specific three-dimensional models? How closely does the virtual result of the osteotomy actually performed match the early postoperative magnetic resonance imaging (MRI)?\n\nParticipants will have a three-dimensional pelvis-acetabulum model created from preoperative MRI. Researchers will perform virtual Salter, Dega, San Diego, and Pemberton osteotomies on that model and measure the resulting acetabular morphology. The virtual result of the osteotomy actually performed will then be compared with the participant's early postoperative MRI.",[26,27,28],"Developmental Dysplasia of the Hip (DDH)","Developmental Dysplasia of the Hip","Acetabular Dysplasia",[30,31,32,33,34,35,36,37,38,39],"Salter osteotomy","Dega osteotomy","San Diego osteotomy","Pemberton osteotomy","Developmental dysplasia of the hip","Acetabular dysplasia","Magnetic resonance imaging","Three dimensional modeling","Acetabular morphometry","Methodological validation","RECRUITING","2026-06-24",{"date":43,"type":44},"2026-06-26","ACTUAL",{"date":46,"type":44},"2026-05-10",{"date":48,"type":22},"2026-10-15",{"name":50,"class":51},"Istanbul University","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":17,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":71,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":4},"100630483","evaluation-of-a-software-application-for-assessment-of-developmental-dysplasia-of-the-hip-100630483","NCT07488260","Evaluation of a Software Application for Assessment of Developmental Dysplasia of the Hip","Evaluation of the Concordance Between the Software Application and Standard Ultrasound Assessment in Classifying Hip Types in Infants Screened for Developmental Dysplasia of the Hip (DDH)","EPA-DDH","Inclusion Criteria:\n\n1. Participants whose Parent(s) or Legally Authorized Representative(s) have provided written informed consent;\n2. Participants who need to undergo routine DDH screening and receive an ultrasound as part of the clinical investigation;\n3. Participants of either sex aged between 4 weeks and 6 months weeks.\n\nExclusion Criteria:\n\n1. Participants with open wounds, ulcers, burns, viral or bacterial infections at the site intended for examination;\n2. Participants with significant anatomical abnormalities (e.g. cerebral palsy, joint contracture, suppurative coxitis, other hip or limb deformities, or teratological hip dysplasia) that may affect the feasibility or accuracy of the examination;\n3. Participants with history of trauma, surgical intervention, or post-traumatic\u002Fpost-surgical condition in the area to be examined.",true,"4 Weeks","6 Months",{"count":65,"type":22},150,"INTERVENTIONAL",[68],"NA","The goal of this prospective, multicentre clinical investigation is to evaluate whether an artificial intelligence (AI)-supported software application can assist clinicians in the diagnostic assessment of developmental dysplasia of the hip (DDH) during routine ultrasound screening in infants.\n\nThe main questions it aims to answer are: Does the diagnostic classification generated by the application agree with the classification obtained by physicians using standard ultrasound examination according to the Graf method? Can the application reliably identify key anatomical landmarks and angles required for DDH assessment?\n\nResearchers will compare the AI-generated diagnostic results with those obtained from standard ultrasound examinations performed by physicians to evaluate the level of agreement between the two approaches.\n\nParticipants will:\n\nundergo a routine hip ultrasound examination performed by a physician according to the Graf method,\n\nhave ultrasound images analyzed by the application,\n\nhave the AI-generated results compared with the physician's assessment.",[26],[27,72,73,74,75],"DDH","Hip Ultrasound","Graf Method","Artificial Intelligence","NOT_YET_RECRUITING","2026-04-02",{"date":79,"type":44},"2026-04-08",{"date":81,"type":22},"2026-07",{"date":83,"type":22},"2027-01",{"name":85,"class":51},"Pentacomp Systemy Informatyczne S.A"]