[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100431621":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":12,"locations":19,"responsibleParty":37,"collaborators":39,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":56,"acronym":7,"eligibilityCriteria":57,"healthyVolunteers":54,"sex":58,"minAge":7,"maxAge":7,"enrollmentInfo":59,"targetDuration":62,"studyType":63,"phases":7,"briefSummary":64,"conditions":65,"keywords":67,"overallStatus":21,"whyStopped":7,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Rett Syndrome Research Trust","OTHER",null,[9],{"name":10,"affiliation":5,"role":11},"Jana von Hehn, PhD","PRINCIPAL_INVESTIGATOR",[13,17],{"name":10,"role":14,"phone":15,"phoneExt":7,"email":16},"CONTACT","203-445-0041","support@rettglobalregistry.org",{"name":18,"role":14,"phone":7,"phoneExt":7,"email":16},"Jennifer Reynolds",[20],{"facility":5,"status":21,"city":22,"state":23,"zip":24,"country":25,"countryCode":26,"cosmosGeoPoint":27,"geoPoint":32,"contacts":33},"RECRUITING","Trumbull","Connecticut","06611","United States","US",{"type":28,"coordinates":29},"Point",[30,31],-73.20067,41.24287,{"lat":31,"lon":30},[34,35],{"name":10,"role":14,"phone":7,"phoneExt":7,"email":16},{"name":36,"role":14,"phone":7,"phoneExt":7,"email":16},"Jenny Reynolds",{"type":38,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR",[40,42,44,46,48,50],{"name":41,"class":6},"Baylor College of Medicine",{"name":43,"class":6},"Vanderbilt University Medical Center",{"name":45,"class":6},"Children's Hospital of Philadelphia",{"name":47,"class":6},"Rush University",{"name":49,"class":6},"Boston Children's Hospital",{"name":51,"class":6},"RTI International","100431621","the-rett-syndrome-global-registry-100431621",false,"NCT04900493","The Rett Syndrome Global Registry","Inclusion Criteria:\n\n1. Parent\u002Fcaregiver must be willing and able to provide written informed consent electronically prior to entering data into the registry.\n2. Rett individuals of any age, living or deceased, must have a diagnosis of Rett syndrome and\u002For have a mutation in MECP2.\n\nExclusion Criteria:\n\n1. Individuals who have a genetic mutation that is inconsistent with Rett syndrome or who have a different disorder.\n2. Individuals with MECP2 Duplication Syndrome","ALL",{"count":60,"type":61},5000,"ESTIMATED","5 Years","OBSERVATIONAL","The Rett Global Registry is a fully remote, global, caregiver-reported registry to collect information about caring for a loved one with Rett syndrome. In addition, caregivers have the ability to track and graph their loved one's symptoms and care strategies over time, store information for central access, and opt-in to complete medical record consolidation and summary. Qualified researchers and therapeutic developers may request access to de-identified aggregate information to further Rett research, or assist with clinical development planning to facilitate and expedite more effective clinical trials.",[66],"Rett Syndrome",[68,69,70],"MECP2","Registry","RSRT","2026-02-12",{"date":73,"type":74},"2026-02-17","ACTUAL",{"date":76,"type":74},"2022-01-31",{"date":78,"type":61},"2031-06-30",{"name":5,"class":6},1]