[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100645460":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":26,"locations":31,"responsibleParty":75,"collaborators":79,"id":85,"slug":86,"hasResults":87,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":91,"eligibilityCriteria":92,"healthyVolunteers":87,"sex":93,"minAge":94,"maxAge":26,"enrollmentInfo":95,"targetDuration":26,"studyType":98,"phases":99,"briefSummary":101,"conditions":102,"keywords":107,"overallStatus":33,"whyStopped":26,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":122},{"fullName":5,"class":6},"Bogomolets National Medical University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"CGM group","EXPERIMENTAL","articipants with prediabetes will be provided with a Real-Time Continuous Glucose Monitoring (RT-CGM) device to monitor their blood glucose along with educational materials to better understand and manage their prediabetes and other supporting services. Pre and post intervention surveys and investigation will be implemented. Participants will be utilizing RT-CGM device for 28 days and then followed up for 3-month participation.",[13],"Device: CGM Sibionics",{"label":15,"type":16,"description":17,"interventionNames":18},"traditional fingerstick glucometer","ACTIVE_COMPARATOR","Participants with prediabetes will be provided with traditional fingerstick glucometer device to self-monitor their blood glucose along with educational materials to better understand and manage their prediabetes and other supporting services. Pre and post intervention surveys and investigation will be implemented. Participants will be utilizing glucometer with at least 2-3 measurements per week for 28 days and then followed up for 3-month participation.",[19],"Device: On-Call Extra Glucometer",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","CGM Sibionics","A registered medical device for real-time monitoring of glucose levels in interstitial fluid.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"On-Call Extra Glucometer","Capillary glucose monitoring using fingerstick glucometer as per standard care.",[15],[32,58,64],{"facility":5,"status":33,"city":34,"state":26,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"RECRUITING","Kyiv","01601","Ukraine","UA",{"type":39,"coordinates":40},"Point",[41,42],30.5238,50.45466,{"lat":42,"lon":41},[45,50,53,55],{"name":46,"role":47,"phone":48,"phoneExt":26,"email":49},"Nazarii Kobyliak, Professor","CONTACT","0442356005","nazariikobyliak@gmail.com",{"name":51,"role":47,"phone":48,"phoneExt":26,"email":52},"Ilona Rudneva, PhD Student","ilonarudneva57@gmail.com",{"name":46,"role":54,"phone":26,"phoneExt":26,"email":26},"PRINCIPAL_INVESTIGATOR",{"name":56,"role":57,"phone":26,"phoneExt":26,"email":26},"Eva Ilkiv, PhD Student","SUB_INVESTIGATOR",{"facility":59,"status":60,"city":34,"state":26,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":61,"geoPoint":63,"contacts":26},"Bogomoletz Institute of Physiology","ENROLLING_BY_INVITATION",{"type":39,"coordinates":62},[41,42],{"lat":42,"lon":41},{"facility":65,"status":33,"city":34,"state":26,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":66,"geoPoint":68,"contacts":69},"University Hospital of Bogomolets National Medical University",{"type":39,"coordinates":67},[41,42],{"lat":42,"lon":41},[70,72],{"name":71,"role":47,"phone":48,"phoneExt":26,"email":52},"Ilona Rudneva, PhD student",{"name":73,"role":47,"phone":48,"phoneExt":26,"email":74},"Victoriia Yerokhovych, PhD","korinnaviktoriaer@gmail.com",{"type":76,"investigatorFullName":77,"investigatorTitle":78,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"SPONSOR_INVESTIGATOR","Nazarii Kobyliak","Vice Rector for Research and Innovation",[80,83],{"name":81,"class":82},"COR-Medical LLC","UNKNOWN",{"name":84,"class":82},"Iridium LLC","100645460","diabetes-glycemic-assessment-in-newly-confirmed-episodes-100645460",false,"NCT07690163","DIabetes GLycemic Assessment in Newly Confirmed Episodes","Evaluation of Continuous Glucose Monitoring Systems for Optimizing Glycemic Control in Patients With Newly Diagnosed Type 2 Diabetes: A Postmarketing Clinical Analysis","DI-GLANCE","Inclusion Criteria:\n\n* Age of 18 years and older.\n* Newly diagnosed Type 2 Diabetes Mellitus according to ADA (American Diabetes Association) criteria (Fasting Plasma Glucose ≥ 7.0 mmol\u002FL, or 2-hour Post-Prandial Glucose ≥ 11.1 mmol\u002FL during OGTT, or HbA1c ≥6.5%).\n* Time since the initial diagnosis of T2D must not exceed 3 months ( less 90 days) at the time of screening.\n* HbA1c level between 6.5% and 9.5% (inclusive) at screening.\n* Patients may be lifestyle-controlled or receiving any stable non-insulin anti-diabetic therapy (including Metformin, SGLT2 inhibitors, GLP-1 receptor agonists, DPP-4 inhibitors, or Sulfonylureas) as monotherapy or combination therapy.\n* Ability to provide written informed consent and willingness to adhere to the study protocol and follow-up schedule.\n\nExclusion Criteria:\n\n* Diagnosis or suspicion of Type 1 Diabetes, Latent Autoimmune Diabetes in Adults (LADA) (e.g., positive anti-GAD antibodies if tested), or secondary types of diabetes (e.g., pancreatic or drug-induced).\n* Any prior or current use of insulin therapy.\n* Severe microvascular or macrovascular complications (proliferative retinopathy, severe diabetic nephropathy with eGFR \\\u003C 45 mL\u002Fmin\u002F1.73m², diabetic foot ulcers, severe peripheral neuropathy).\n* Endocrine disorders (e.g., Itsenko-Cushing syndrome, acromegaly) that affect glycemia.\n* History of myocardial infarction, stroke, unstable angina, coronary artery bypass graft (CABG), or percutaneous coronary intervention (PCI) within the past 6 months.\n* Active malignancy, decompensated heart failure (NYHA Class III or IV), or chronic infectious diseases.\n* Pregnant or breastfeeding women, or women of childbearing potential not using highly effective contraception.\n* Has evidence of current abuse of drugs or alcohol or a history of abuse that, in the investigator's opinion, would cause the individual to be noncompliant.\n* Participation in another clinical study within the last 3 months.","ALL","18 Years",{"count":96,"type":97},80,"ESTIMATED","INTERVENTIONAL",[100],"NA","This is a prospective, open-label, randomized controlled trial involving 80 adult patients with newly diagnosed T2DM (diagnosed within the last 3 months) recruited at the Bogomolets National Medical University. Participants may be lifestyle-controlled or receiving stable non-insulin anti-diabetic medications. Participants will be randomized in a 1:1 ratio to either the Real-Time Continuous Glucose Monitoring group (CGM group) or the control group (standard Self-Monitoring of Blood Glucose \\[SMBG\\] using conventional glucometers).\n\nThe gathered data will help determine whether the real-time visual feedback provided by CGM systems superiorly improves glycemic variability, optimizes metabolic parameters, and enhances patient adherence to lifestyle interventions and pharmacological treatment compared to conventional SMBG methods in the early stages of T2D.",[103,104,105,106],"Type 2 Diabetes (T2DM)","Obesity Type 2 Diabetes Mellitus","Obesity & Overweight","Insulin Resistance",[108,109,110,111,112],"obesity","continuous glucose monitoring","insulin resistance","traditional glycemia self-monitoring","type 2 diabetes","2026-07-11",{"date":115,"type":116},"2026-07-14","ACTUAL",{"date":118,"type":97},"2026-07-15",{"date":120,"type":97},"2027-03-31",{"name":77,"class":6},3]