[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100362758":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":18,"centralContacts":23,"locations":32,"responsibleParty":49,"collaborators":10,"id":51,"slug":52,"hasResults":53,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":10,"eligibilityCriteria":57,"healthyVolunteers":53,"sex":58,"minAge":10,"maxAge":10,"enrollmentInfo":59,"targetDuration":62,"studyType":63,"phases":10,"briefSummary":64,"conditions":65,"keywords":67,"overallStatus":34,"whyStopped":10,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":82},{"fullName":5,"class":6},"Newcastle University","OTHER",[8],{"label":9,"type":10,"description":10,"interventionNames":11},"Participants with Myotonic Dystrophy",null,[12],"Other: Patient Registry",[14],{"type":6,"name":15,"description":16,"armGroupLabels":17,"otherNames":10},"Patient Registry","Participants who have volunteered to participate will complete various questionnaires relating to their condition.",[9],[19],{"name":20,"affiliation":21,"role":22},"Chiara Marini-Bettolo, MD, PhD","John Walton Muscular Dystrophy Research Centre","PRINCIPAL_INVESTIGATOR",[24,29],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},"Registry Project Manager and Curator","CONTACT","0191 2418640","helen.walker2@newcastle.ac.uk",{"name":30,"role":26,"phone":10,"phoneExt":10,"email":31},"Registries Team","registries@ncl.ac.uk",[33],{"facility":21,"status":34,"city":35,"state":10,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"RECRUITING","Newcastle upon Tyne","NE1 3BZ","United Kingdom","UK",{"type":40,"coordinates":41},"Point",[42,43],-1.61396,54.97328,{"lat":43,"lon":42},[46,48],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":47},"myotonicdystrophyregistry@newcastle.ac.uk",{"name":20,"role":22,"phone":10,"phoneExt":10,"email":10},{"type":50,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100362758","the-united-kingdom-national-registry-for-myotonic-dystrophy-100362758",false,"NCT04003363","The United Kingdom National Registry for Myotonic Dystrophy","The UK National Registry for Myotonic Dystrophy","Inclusion Criteria:\n\n* All patients with a confirmed Myotonic Dystrophy diagnosis (or pending diagnosis) are eligible for inclusion. Diagnosis will be confirmed via genetic testing results\n\nExclusion Criteria:\n\n* There are no exclusion criteria for the registry","ALL",{"count":60,"type":61},900,"ESTIMATED","20 Years","OBSERVATIONAL","Myotonic dystrophy (dystrophia myotonica - DM) exists in two forms, usually referred to as DM1 (type 1) and DM2 (type 2). Both conditions are genetic disorders but each affects a different gene. DM1 is the most common adult-onset muscular dystrophy, and is thought to affect at least 1 in 8,000 people worldwide.\n\nThe aim is to facilitate a questionnaire based research study in order to better characterise and understand the disease in the UK. By maintaining a national registry this will help identify potential participants eligible for clinical trials in the future.",[66],"Myotonic Dystrophy",[66,68,69,70,71,72],"Myotonic Dystrophy Type 1","Myotonic Dystrophy Type 2","DM","DM1","DM2","2023-11-28",{"date":75,"type":76},"2023-12-04","ACTUAL",{"date":78,"type":76},"2013-05",{"date":80,"type":61},"2030-12",{"name":5,"class":6},1]