[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"World Federation of Hemophilia\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":17,"targetDuration":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100310930","world-bleeding-disorders-registry-100310930",false,"NCT03327779","World Bleeding Disorders Registry","WBDR","Inclusion Criteria:\n\n* Patients of participating Hemophilia Treatment Centres with Hemophilia A or B, or von Willebrand Disease\n\nExclusion Criteria:\n\n* none","ALL",{"count":18,"type":19},20000,"ESTIMATED","5 Years","OBSERVATIONAL","The WBDR is an international observational disease registry of patients with hemophilia. It will provide a platform for a network of hemophilia treatment centres (HTCs) around the world to collect uniform and standardized patient data and guide clinical practice. With informed consent from the patient, the WBDR stores anonymous data about the person's disease, such as hemophilia type and severity, symptoms, and treatment.",[24,25,26],"Hemophilia A","Hemophilia B","Von Willebrand Diseases","RECRUITING","2023-08-07",{"date":30,"type":31},"2023-08-14","ACTUAL",{"date":33,"type":31},"2018-01-26",{"date":35,"type":19},"2028-01",{"name":37,"class":38},"World Federation of Hemophilia","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":48,"enrollmentInfo":49,"targetDuration":48,"studyType":21,"phases":4,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":4},"100430333","the-world-federation-of-hemophilia-gene-therapy-registry-100430333","NCT04883710","The World Federation of Hemophilia Gene Therapy Registry","WFH GTR","Inclusion Criteria:\n\n* People with hemophilia who have received a gene therapy product\n\nExclusion Criteria:\n\n* None","0 Years","100 Years",{"count":50,"type":19},5000,"The aim of the WFH GTR is to provide a database in which long-term data on PWH who receive gene therapy from around the world, will be collected and housed.",[53],"Hemophilia",[55],"Gene therapy","NOT_YET_RECRUITING","2021-05-11",{"date":59,"type":31},"2021-05-12",{"date":61,"type":19},"2022-01-01",{"date":63,"type":19},"2050-01-01",{"name":37,"class":38},""]