[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100622823":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":13,"locations":23,"responsibleParty":46,"collaborators":7,"id":48,"slug":7,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":49,"sex":55,"minAge":56,"maxAge":7,"enrollmentInfo":57,"targetDuration":60,"studyType":61,"phases":7,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":26,"whyStopped":7,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"fullName":5,"class":6},"Artcline GmbH","INDUSTRY",null,[9],{"name":10,"affiliation":11,"role":12},"Martin Sauer, Prof. Dr. med.","Klinikum Magdeburg, Klinik für Intensiv- & Rettungsmedizin","PRINCIPAL_INVESTIGATOR",[14,19],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},"Jens Altrichter, Dr. med.","CONTACT","+49 381 440 703 0","jens.altrichter@artcline.de",{"name":20,"role":16,"phone":21,"phoneExt":7,"email":22},"Judith Gross, M. Sc.","+49 1772216033","judith.gross@artcline.de",[24],{"facility":25,"status":26,"city":27,"state":7,"zip":28,"country":29,"countryCode":30,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"Klinikum Magdeburg, Klinik für Intensiv- und Rettungsmedizin","RECRUITING","Magdeburg","39130","Germany","DE",{"type":32,"coordinates":33},"Point",[34,35],11.63189,52.13129,{"lat":35,"lon":34},[38,43],{"name":39,"role":16,"phone":40,"phoneExt":41,"email":42},"Martin Sauer, Pof. Dr.","+49391791","3105","martin.sauer@klinikum-magdeburg.de",{"name":44,"role":16,"phone":40,"phoneExt":41,"email":45},"Georg Richter","georg.richter@Klinikum-Magdeburg.de",{"type":47,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100622823",false,"NCT07388628","ARTICE® Real Data Collection & Observational Trial, Phase 4 Study","ARTISTRY - ARTICE® Therapy Registry Study","ARTistry","Inclusion Criteria:\n\n* Subjects ≥ 18 years who are planned to receive ARTICE® treatment during their ICU stay\n\nExclusion Criteria:\n\n\\-","ALL","18 Years",{"count":58,"type":59},200,"ESTIMATED","7 Days","OBSERVATIONAL","The objectives of this registry study are to:\n\n1. Record real-life data related to the use of the ARTICE® therapy in sepsis subjects.\n2. Further evaluate ARTICE® treatment efficacy.\n3. Identify potential sub-groups, assess their risk-benefit- and safety profile.\n4. Changes in SOFA score D0 to SOFA Score D7.",[64,65,66],"Sepsis","Septic Shock","Immunoparalysis in Septic Shock",[64,68,66],"septic shock","2026-02-06",{"date":71,"type":72},"2026-02-09","ACTUAL",{"date":74,"type":72},"2025-09-25",{"date":76,"type":59},"2027-12",{"name":5,"class":6},1]