[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100543945":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":12,"centralContacts":17,"locations":23,"responsibleParty":45,"collaborators":7,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":49,"sex":54,"minAge":7,"maxAge":7,"enrollmentInfo":55,"targetDuration":58,"studyType":59,"phases":7,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":26,"whyStopped":7,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":76},{"fullName":5,"class":6},"Fondazione SISA (Societa Italiana per lo Studio della Arteriosclerosi)","OTHER",null,[9],{"type":10,"name":11,"description":7,"armGroupLabels":7,"otherNames":7},"DRUG","Lipid-lowering treatments",[13],{"name":14,"affiliation":15,"role":16},"Alberico L Catapano, PhD","Fondazione S.I.S.A.","STUDY_CHAIR",[18],{"name":19,"role":20,"phone":21,"phoneExt":7,"email":22},"Manuela Casula, PhD","CONTACT","0039 + 0250318428","manuela.casula@unimi.it",[24],{"facility":25,"status":26,"city":27,"state":28,"zip":29,"country":30,"countryCode":31,"cosmosGeoPoint":32,"geoPoint":37,"contacts":38},"IRCCS Multimedica","RECRUITING","Sesto San Giovanni","Milano","20099","Italy","IT",{"type":33,"coordinates":34},"Point",[35,36],9.22585,45.53329,{"lat":36,"lon":35},[39,43],{"name":40,"role":20,"phone":41,"phoneExt":7,"email":42},"Fabio Pellegatta, MD","00390224209593","lipigen@sisa.it",{"name":40,"role":44,"phone":7,"phoneExt":7,"email":7},"PRINCIPAL_INVESTIGATOR",{"type":46,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100543945","lipid-transport-disorder-italian-genetic-record-lipigen-100543945",false,"NCT06362473","Lipid Transport Disorder Italian Genetic Record (LIPIGEN)","LIPIGEN","Inclusion Criteria:\n\n* Molecular or clinical diagnosis of genetic dyslipidemia\n* Informed consent signed\n\nExclusion Criteria:\n\n* None","ALL",{"count":56,"type":57},10000,"ESTIMATED","10 Years","OBSERVATIONAL","LIPIGEN is an observational study involving Italian physicians and researchers in the field of diseases related to blood lipid levels. This study aims to improve the diagnosis and treatment of people with familial dyslipidaemias, including very common conditions such as familial hypercholesterolaemia (FH) and less common ones such as familial chylomicronidaemic syndrome (FCS).\n\nWhat does the study do?\n\nIt collects information on Italian patients with Familial Hypercholesterolaemia (FH), following them in their normal clinical examination without adding extra procedures.\n\nIt uses the data collected to further our understanding of diseases such as familial hypercholesterolaemia, examining how it is diagnosed clinically and by genetic testing, and evaluating the effectiveness of different treatments.\n\nIt seeks to identify the genetic mutations that cause familial hypercholesterolaemia and other dyslipidaemias, helping to choose the most effective treatments.\n\nIt evaluates the impact of long-term treatments and patient adherence to medication, as well as monitoring the incidence of cardiovascular events and other important outcomes.\n\nWho can participate?\n\nThe study is aimed at people of all ages, from children to adults, with familial hypercholesterolaemia or other genetic dyslipidaemia.\n\nMore than 50 centres throughout Italy are involved, making the study accessible to many.\n\nWhat does participation entail?\n\nParticipants will continue with their normal clinical practice.\n\nData such as family history, personal clinical findings and genetic information will be collected, without additional procedures.\n\nFor some, further evaluations, such as ultrasounds, may be required to better study their condition.\n\nThe LIPIGEN study not only helps to better understand diseases related to high cholesterol but also aims to improve patients\\' lives through more precise diagnosis and personalised treatments.",[62,63],"Familial Hypercholesterolemia","Genetic Disorder",[52,65,66],"Familial Hypercholesterelomia","Genetic Dyslipidemia","2024-04-08",{"date":69,"type":70},"2024-04-12","ACTUAL",{"date":72,"type":70},"2015-08-04",{"date":74,"type":57},"2026-09-30",{"name":5,"class":6},1]