[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100624795":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":40,"responsibleParty":85,"collaborators":87,"id":92,"slug":93,"hasResults":94,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":98,"eligibilityCriteria":99,"healthyVolunteers":94,"sex":100,"minAge":101,"maxAge":102,"enrollmentInfo":103,"targetDuration":26,"studyType":106,"phases":107,"briefSummary":109,"conditions":110,"keywords":112,"overallStatus":43,"whyStopped":26,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":124},{"fullName":5,"class":6},"Shanghai 6th People's Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention group (RT-CGM Group)","EXPERIMENTAL","Participants in this group will use a Real-Time Continuous Glucose Monitoring (RT-CGM) system intermittently during the 12-week intervention period, followed by a 14-week follow-up period.",[13],"Device: RT-CGM",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group (SMBG Group)","ACTIVE_COMPARATOR","Participants in this group will perform standard Self-Monitoring of Blood Glucose (SMBG) using a blood glucose meter throughout the 12-week intervention period, followed by a 14-week follow-up period.",[19],"Device: SMBG",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","RT-CGM","RT-CGM can provide real-time tracking of glucose levels, and offer glucose trend graphs and user-configurable low and high glucose alerts.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"SMBG","SMBG provides discrete, point-in-time capillary blood glucose measurements via fingerstick testing.",[15],[32],{"name":33,"affiliation":5,"role":34},"Jian Zhou","PRINCIPAL_INVESTIGATOR",[36],{"name":33,"role":37,"phone":38,"phoneExt":26,"email":39},"CONTACT","86-21-64369181","zhoujian@sjtu.edu.cn",[41,59,65,75],{"facility":42,"status":43,"city":44,"state":26,"zip":45,"country":46,"countryCode":47,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"Shanghai 7th People's Hospital","RECRUITING","Shanghai","200137","China","CN",{"type":49,"coordinates":50},"Point",[51,52],121.45806,31.22222,{"lat":52,"lon":51},[55],{"name":56,"role":37,"phone":57,"phoneExt":26,"email":58},"Xiaohua Li","021-58670561","13816805177@163.com",{"facility":5,"status":43,"city":44,"state":26,"zip":26,"country":46,"countryCode":47,"cosmosGeoPoint":60,"geoPoint":62,"contacts":63},{"type":49,"coordinates":61},[51,52],{"lat":52,"lon":51},[64],{"name":33,"role":37,"phone":38,"phoneExt":26,"email":39},{"facility":66,"status":43,"city":44,"state":26,"zip":26,"country":46,"countryCode":47,"cosmosGeoPoint":67,"geoPoint":69,"contacts":70},"Shanghai Fengxian District Central Hospital",{"type":49,"coordinates":68},[51,52],{"lat":52,"lon":51},[71],{"name":72,"role":37,"phone":73,"phoneExt":26,"email":74},"Peihong Chen","86+18018820016","cph502@163.com",{"facility":76,"status":43,"city":44,"state":26,"zip":26,"country":46,"countryCode":47,"cosmosGeoPoint":77,"geoPoint":79,"contacts":80},"Shanghai General Hospital",{"type":49,"coordinates":78},[51,52],{"lat":52,"lon":51},[81],{"name":82,"role":37,"phone":83,"phoneExt":26,"email":84},"Yufan Wang","86+13761675784","yyffwang@sina.com",{"type":34,"investigatorFullName":33,"investigatorTitle":86,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Principal Investigator, Professor, Chief Physician, Director",[88,90,91],{"name":89,"class":6},"Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine",{"name":66,"class":6},{"name":42,"class":6},"100624795","cgm-for-insulin-treated-t2dm-during-post-discharge-transition-100624795",false,"NCT07414277","CGM for Insulin-Treated T2DM During Post-Discharge Transition","Effects of Continuous Glucose Monitoring on Patients With Type 2 Diabetes Treated With Insulin During Post-Discharge Transition: A Multicenter Randomized Controlled Trial","TRANSIT-CGM","Inclusion Criteria:\n\n1. Age 18 to 80 years (inclusive).\n2. Confirmed diagnosis of type 2 diabetes mellitus (T2DM).\n3. HbA1c between 8.0% and 13.0% (inclusive) within the last 1 month prior to screening\u002Fenrollment.\n4. Planned to receive insulin therapy for at least 6 months after hospital discharge, as assessed\u002Fconfirmed by the treating physician (principal physician).\n\nExclusion Criteria:\n\n1. Current use of a real-time continuous glucose monitoring (RT-CGM) device, or use within the 3 months prior to enrollment.\n2. Severe skin disease at the sensor insertion site, or allergy to adhesive tape\u002Fadhesives.\n3. Pregnant women; positive pregnancy test at screening; or planning pregnancy during the study period.\n4. Currently participating in, or planning to participate in, another clinical trial.\n5. Current use of oral corticosteroid therapy, or anticipated use during the trial period.\n6. Severe liver disease, defined as alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \\>3 times the upper limit of normal (ULN).\n7. Severe renal impairment or end-stage renal disease, defined as estimated glomerular filtration rate (eGFR) \\\u003C30 mL\u002Fmin\u002F1.73 m².\n8. Any condition that, in the investigator's opinion, makes the participant unsuitable for the trial, for example: history of ocular trauma or other diagnosed eye diseases causing visual impairment; unwillingness to participate or inability to adequately understand\u002Fcomply due to speech\u002Flanguage impairment; or presence of psychiatric disorders.","ALL","18 Years","80 Years",{"count":104,"type":105},160,"ESTIMATED","INTERVENTIONAL",[108],"NA","The transition from inpatient care to the home setting is a critical phase for glycemic management, often associated with decreased adherence and deterioration of glycemic control. This multicenter, randomized, open-label, controlled trial aims to evaluate the efficacy of Real-Time Continuous Glucose Monitoring (RT-CGM) versus Self-Monitoring of Blood Glucose (SMBG) in patients with Type 2 Diabetes Mellitus (T2DM) treated with insulin during the post-discharge transitional period.\n\nA total of 160 eligible participants will be randomized in a 1:1 ratio to either the RT-CGM group or the SMBG group. Participants will wear RT-CGM intermittently (every 4 weeks) or perform SMBG for the 12-week intervention period. They will also visit the clinic at Week 12 and Week 24 for follow-up assessments.",[111],"Type 2 Diabetes Mellitus (T2DM)",[113,114],"continuous glucose monitoring","insulin-treated","2026-06-21",{"date":117,"type":118},"2026-06-24","ACTUAL",{"date":120,"type":118},"2026-05-11",{"date":122,"type":105},"2027-12-31",{"name":5,"class":6},4]