[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Luca Sangiorgi\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":128},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,43,67,89,109],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100458286","data-collection-of-patients-with-rare-bone-diseases-100458286",false,"NCT05247645","Data Collection of Patients With Rare Bone Diseases","Structured Collection of Data Relating to Rare Diseases With Predominantly Skeletal Involvement","RD-DATA","Inclusion Criteria:\n\n* All patients affected by rare diseases with predominantly skeletal involvement\n\nExclusion Criteria:\n\n* Any condition unrelated to rare diseases with predominantly skeletal involvement","ALL",{"count":19,"type":20},1000,"ESTIMATED","OBSERVATIONAL","RD-DATA is a retrospective and prospective data collection, finalized for care and research purposes. It is articulated in main sections - strongly related and mutually dependent on each other - corresponding to different data domains: personal information, clinical data, genetic data, genealogical data, surgeries, etc.\n\nThis approach has been developed to corroborate and integrate data from different sources and evaluating several aspects of the diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate diseases pathophysiology. Due to legal requirements, institutional directives and organizational issues, we are unable to include individuals residing outside Italy in the registry at this time. We are currently engaged in the preparation of a recruitment process for individuals residing outside Italy.",[24],"Skeletal Dysplasia",[26,27,28,29],"Rare Disease with predominantly skeletal involvement","Disease Evolution","Data Collection","Natural History Study","RECRUITING","2025-11-17",{"date":33,"type":34},"2025-11-20","ACTUAL",{"date":36,"type":34},"2020-10-10",{"date":38,"type":20},"2045-10-09",{"name":40,"class":41},"Luca Sangiorgi","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":52,"targetDuration":54,"studyType":21,"phases":4,"briefSummary":55,"conditions":56,"keywords":59,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":61,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":42},"100372834","registry-of-ollier-disease-and-maffucci-syndrome-100372834","NCT04134572","Registry of Ollier Disease and Maffucci Syndrome","Registry of Ollier Disease and Maffucci Syndrome That Collects Clinical, Functional, Genetic, Genealogical, Imaging, Surgical, Treatment, Quality of Life Data. Data is Linked to Patients' Biological Samples, When Available","ROM","Inclusion Criteria:\n\n* All patients affected by Ollier Disease and Maffucci Syndrome\n\nExclusion Criteria:\n\n* Any condition unrelated to Ollier Disease and\u002For Maffucci Syndrome",true,{"count":53,"type":20},400,"25 Years","REM is a retrospective and prospective registry, finalized to care and research. It is articulated in main sections - strongly related and mutually dependent on each other - corresponding to different data domains: personal information, clinical data, genetic data, genealogical data, surgeries, etc..\n\nThis approach has been individuated in order to corroborate and integrate data from different resources and aspects of the diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate diseases pathophysiology. Due to legal requirements, institutional directives and organizational issues, we are unable to include individuals residing outside Italy in the registry at this time. We are currently engaged in the preparation of a recruitment process for individuals residing outside Italy.",[57,58],"Ollier Disease","Maffucci Syndrome",[60,29,27],"Disease Registry",{"date":33,"type":34},{"date":63,"type":34},"2017-01-16",{"date":65,"type":20},"2032-01",{"name":40,"class":41},{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":73,"eligibilityCriteria":74,"healthyVolunteers":51,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":75,"targetDuration":54,"studyType":21,"phases":4,"briefSummary":77,"conditions":78,"keywords":80,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":83,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":42},"100372736","registry-of-multiple-osteochondromas-100372736","NCT04133285","Registry of Multiple Osteochondromas","Registry of Multiple Osteochondromas That Collects Clinical, Functional, Genetic, Genealogical, Imaging, Surgical, Treatment, Quality of Life Data. Data is Linked to Patients' Biological Samples, When Available.","REM","Inclusion Criteria:\n\n* All Multiple Osteochondromas patients, including prenatal diagnosis of Multiple Osteochondromas\n\nExclusion Criteria:\n\n* Any condition unrelated to Multiple Osteochondromas",{"count":76,"type":20},10000,"REM is a retrospective and prospective registry, finalized for care and research purposes. It is articulated in main sections - strongly related and mutually dependent on each other - corresponding to different data domains: personal information, clinical data, genetic data, genealogical data, surgeries, etc.\n\nThis approach has been developed to corroborate and integrate data from different sources evaluating several aspects of diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate disease pathophysiology. Due to legal requirements, institutional directives and organizational issues, we are unable to include individuals residing outside Italy in the registry at this time. We are currently engaged in the preparation of a recruitment process for individuals residing outside Italy.",[79],"Multiple Osteochondromas",[60,29,81,82],"Disease evolution","Genotype-Phenotype Correlation",{"date":33,"type":34},{"date":85,"type":34},"2013-06-28",{"date":87,"type":20},"2032-12",{"name":40,"class":41},{"id":90,"slug":91,"hasResults":11,"nctId":92,"briefTitle":93,"officialTitle":94,"acronym":95,"eligibilityCriteria":96,"healthyVolunteers":51,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":97,"targetDuration":54,"studyType":21,"phases":4,"briefSummary":99,"conditions":100,"keywords":102,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":103,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":42},"100372735","registry-of-ehlers-danlos-syndrome-100372735","NCT04133272","Registry of Ehlers-Danlos Syndrome","Registry of Ehlers-Danlos Syndrome That Collects Clinical, Functional, Genetic, Genealogical, Imaging, Surgical, Treatment, Quality of Life Data. Data Are Linked to Patients' Biological Samples, When Available","RED","Inclusion Criteria:\n\n* All Ehlers-Danlos Syndrome patients, including prenatal and fetal diagnosis of Ehlers-Danlos Syndrome\n\nExclusion Criteria:\n\n* Any condition unrelated to Ehlers-Danlos Syndrome",{"count":98,"type":20},3000,"RED is a retrospective and prospective registry, finalized for care and research purposes. It is articulated in main sections - strongly related and mutually dependent on each other - corresponding to different data domains: personal information, clinical data, genetic data, genealogical data, surgeries, etc.\n\nThis approach has been developed to corroborate and integrate data from different sources and evaluating several aspects of diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate disease pathophysiology. Due to legal requirements, institutional directives and organizational issues, we are unable to include individuals residing outside Italy in the registry at this time. We are currently engaged in the preparation of a recruitment process for individuals residing outside Italy.",[101],"Ehlers-Danlos Syndrome",[60,29,27,82],{"date":33,"type":34},{"date":105,"type":34},"2014-06",{"date":107,"type":20},"2033-01",{"name":40,"class":41},{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":115,"eligibilityCriteria":116,"healthyVolunteers":51,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":117,"targetDuration":54,"studyType":21,"phases":4,"briefSummary":119,"conditions":120,"keywords":122,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":123,"startDateStruct":124,"completionDateStruct":125,"leadSponsor":127,"locationsCount":42},"100371392","registry-of-osteogenesis-imperfecta-100371392","NCT04115774","Registry of Osteogenesis Imperfecta","Registry of Osteogenesis Imperfecta That Collects Clinical, Functional, Genetic, Genealogical, Imaging, Surgical, Quality of Life Data. Data is Linked to Patients Biological Samples, When Available","ROI","Inclusion Criteria:\n\n* All Osteogenesis Imperfecta patients, including prenatal and fetal diagnosis of Osteogenesis Imperfecta\n\nExclusion Criteria:\n\n* Any condition unrelated to Osteogenesis Imperfecta",{"count":118,"type":20},5000,"ROI is a retrospective and prospective registry, finalized for care and research purposes. It is articulated in main sections - strongly related and mutually dependent on each other - corresponding to different data domains: personal information, clinical data, genetic data, genealogical data, surgeries, etc. This approach has been developed to corroborate and integrate data from different sources evaluating several aspects of diseases and to correlate genetic background and phenotypic outcomes, in order to better investigate diseases pathophysiology. Due to legal requirements, institutional directives and organizational issues, we are unable to include individuals residing outside Italy in the registry at this time. We are currently engaged in the preparation of a recruitment process for individuals residing outside Italy.",[121],"Osteogenesis Imperfecta",[60,29,27,82],{"date":33,"type":34},{"date":85,"type":34},{"date":126,"type":20},"2032-02-29",{"name":40,"class":41},""]