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Strasbourg","Strasbourg",{"type":26,"coordinates":250},[251,252],7.74553,48.58392,{"lat":252,"lon":251},{"facility":255,"status":10,"city":256,"state":10,"zip":10,"country":23,"countryCode":24,"cosmosGeoPoint":257,"geoPoint":261,"contacts":10},"CHU Toulouse (Rangueil)","Toulouse",{"type":26,"coordinates":258},[259,260],1.44367,43.60426,{"lat":260,"lon":259},{"facility":263,"status":10,"city":264,"state":10,"zip":10,"country":23,"countryCode":24,"cosmosGeoPoint":265,"geoPoint":269,"contacts":10},"CHU Tours","Tours",{"type":26,"coordinates":266},[267,268],0.70398,47.39484,{"lat":268,"lon":267},{"type":271,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100386174","the-minimed-780g-glycemic-control-and-quality-of-life-study-for-the-treatment-of-pediatric-and-adult-subjects-with-type-1-diabetes-in-france-100386174",true,"NCT04308291","The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment of Pediatric and Adult Subjects With Type 1 Diabetes in France.","The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment of Pediatric and Adult Subjects With Type 1 Diabetes in France (EQOL Study)","Inclusion Criteria:\n\n1. Subject is ≥7 years of age.\n2. Subject has a clinical diagnosis of type 1 diabetes for more than 1 year as determined via medical records or source documentation by an individual qualified to make a medical diagnosis.\n3. Subject has a HbA1c value greater than 6.5% and less than 12% at time of enrolment visit.\n4. Subject is under Continuous Subcutaneous Insulin Infusion (CSII) therapy (with or without Continuous Glucose Monitoring) ≥ 6 months before enrolment.\n5. Subject requires ≥8 units of insulin per day.\n6. Subjects and their parent(s)\u002Fguardian(s) must be able to speak and be literate in French as verified by the investigator.\n7. Subjects and their parent(s)\u002Fguardian(s) are willing to participate in the study and sign the Data Release Form (DRF).\n8. Subjects who are ≥18 years of age should be able to provide consent.\n\nExclusion Criteria:\n\n1. Subject has MiniMed™ 780G System IFU contraindication(s).\n2. Subject uses Predictive Low-Glucose Management (PLGM) System (i.e. MiniMed™ 640G with SmartGuard) in the last 6 months before the enrolment.\n3. Subject uses Low Glucose suspend (LGS) feature (i.e. MiniMed™ Paradigm Veo Pump) in the last 6 months before the enrolment.\n4. Subject under Multiple-Daily Injections (MDI) treatment in the 6 months before the enrolment.\n5. Subject has any unresolved adverse skin condition in the area of sensor placement (e.g., psoriasis, dermatitis herpetiformis, rash, Staphylococcus infection).",false,"ALL","7 Years",{"count":283,"type":284},306,"ACTUAL","OBSERVATIONAL","The purpose of the study is to evaluate the efficacy in glycemic control and the impact on the quality of life of patients using the MiniMed™ 780G System for the treatment of Type 1 diabetes, in real life settings in France.",[288],"Type 1 Diabetes",[290],"780G, T1D","COMPLETED","2024-01-09",{"date":294,"type":284},"2024-07-08",{"date":296,"type":284},"2021-02-15",{"date":298,"type":284},"2022-10-27",{"name":5,"class":6},32]