[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100418711":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":15,"centralContacts":20,"locations":29,"responsibleParty":70,"collaborators":7,"id":72,"slug":73,"hasResults":74,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":77,"eligibilityCriteria":78,"healthyVolunteers":74,"sex":79,"minAge":7,"maxAge":7,"enrollmentInfo":80,"targetDuration":7,"studyType":83,"phases":7,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":32,"whyStopped":7,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"University of Bern","OTHER",null,[9,12],{"type":6,"name":10,"description":11,"armGroupLabels":7,"otherNames":7},"Physical examination, diagnostic tests, laboratory tests","Physical examination, diagnostic tests depending on examined organ system (e.g. lung function test, echocardiography, audiometry), and laboratory tests (e.g. kidney parameter, hormonal levels).",{"type":6,"name":13,"description":14,"armGroupLabels":7,"otherNames":7},"Personal history, questionnaire","Personal history and focused questionnaires per organ system including symptoms, medication use, physical activity, and general wellbeing.",[16],{"name":17,"affiliation":18,"role":19},"Claudia E Kuehni, MD","Institute of Social and Preventive Medicine, University of Bern","PRINCIPAL_INVESTIGATOR",[21,25],{"name":17,"role":22,"phone":23,"phoneExt":7,"email":24},"CONTACT","+41 31 631 35 07","claudia.kuehni@unibe.ch",{"name":26,"role":22,"phone":27,"phoneExt":7,"email":28},"Maša Žarković, MD","+41 31 684 68 58","masa.zarkovic@unibe.ch",[30,46,58],{"facility":31,"status":32,"city":33,"state":7,"zip":7,"country":34,"countryCode":35,"cosmosGeoPoint":36,"geoPoint":41,"contacts":42},"University Childen's Hospital Basel","RECRUITING","Basel","Switzerland","CH",{"type":37,"coordinates":38},"Point",[39,40],7.57327,47.55839,{"lat":40,"lon":39},[43,45],{"name":44,"role":22,"phone":7,"phoneExt":7,"email":7},"Nicolas X von der Weid, MD",{"name":44,"role":19,"phone":7,"phoneExt":7,"email":7},{"facility":47,"status":32,"city":48,"state":7,"zip":7,"country":34,"countryCode":35,"cosmosGeoPoint":49,"geoPoint":53,"contacts":54},"University Children's Hospital Bern","Bern",{"type":37,"coordinates":50},[51,52],7.44744,46.94809,{"lat":52,"lon":51},[55,57],{"name":56,"role":22,"phone":7,"phoneExt":7,"email":7},"Philipp Latzin, MD",{"name":56,"role":19,"phone":7,"phoneExt":7,"email":7},{"facility":59,"status":32,"city":60,"state":7,"zip":7,"country":34,"countryCode":35,"cosmosGeoPoint":61,"geoPoint":65,"contacts":66},"University Hospital Geneva","Geneva",{"type":37,"coordinates":62},[63,64],6.14569,46.20222,{"lat":64,"lon":63},[67,69],{"name":68,"role":22,"phone":7,"phoneExt":7,"email":7},"Marc Ansari, MD",{"name":68,"role":19,"phone":7,"phoneExt":7,"email":7},{"type":71,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100418711","the-swiss-childhood-cancer-survivor-study---follow-up-sccss-followup-100418711",false,"NCT04732273","The Swiss Childhood Cancer Survivor Study - Follow-up (SCCSS-FollowUp)","SCCSS-FU","This prospective cohort study is based on the Childhood Cancer Registry (ChCR), a national, population-based cancer registry that includes all children and adolescents in Switzerland who were diagnosed with cancer at age 0-20 years. It includes patients diagnosed with leukemia, lymphoma, central nervous system tumors, and malignant solid tumors or Langerhans cell histiocytosis.\n\nInclusion Criteria:\n\n* Registered in the Childhood Cancer Registry (ChCR) or treated and followed-up in a Swiss pediatric oncology (SPOG) clinic, but not registered in the ChCR because of residency in neighboring countries\n* Diagnosed at age 0 - 20 years\n* Childhood cancer treatment completed\n* All age categories at time of inclusion in the study (children, adolescents, adults)\n* Written informed consent\n\nExclusion criteria:\n\n* Childhood cancer survivors in a palliative or relapsed situation where no follow-up examinations are foreseen.","ALL",{"count":81,"type":82},3000,"ESTIMATED","OBSERVATIONAL","The SCCSS-FollowUp is a national, multicenter cohort study designed to investigate late effects in childhood cancer survivors in a prospective and longitudinal way. The study is embedded in regular follow-up care and inclusion in the study takes place in a step-wise approach. The investigators collect data from clinical examinations, laboratory and functional tests, and questionnaires to learn more about late effects of childhood cancer treatments.",[86,87],"Late Effect","Childhood Cancer",[87,89,90],"Late Effects","Survivor","2025-09-18",{"date":93,"type":94},"2025-09-23","ACTUAL",{"date":96,"type":94},"2022-06-20",{"date":98,"type":82},"2071-01-01",{"name":5,"class":6},3]