Phase
Condition
Diabetes Prevention
Diabetes Mellitus Types I And Ii
Diabetes Mellitus, Type 1
Treatment
Capillary Blood glucose Testing (POC)
Dexcom G7 rtCGM
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Known history of T1D treated with insulin therapy (human regular or rapid-actinganalogs or ultra-rapid analogs [lispro, aspart, glulisine, fast-acting insulinaspart, insulin lispro]), intermediate-acting (NPH and premixed formulations) orlong-acting basal (glargine, detemir, degludec) formulations.
Admission diagnosis of T1D with poorly controlled diabetes (blood glucose > 180mg/dl, HbA1c > 7%), including diabetic ketoacidosis (DKA) and hyperglycemichyperosmolar state (HHS).
Expected length of hospital stay > three days at the time of randomization
Exclusion
Exclusion Criteria:
Patients admitted to the ICU
Subjects using CGM technology before admission
Subjects with type 2 diabetes
Treatment with systemic immunosuppressive agents
Cystic fibrosis
Prisoners
Patients expected to require MRI procedures during hospitalization.
Female subjects who are pregnant or breastfeeding at enrollment into the study.
Subjects not willing to wear a CGM device
Subjects with clinically relevant hepatic disease (diagnosed liver cirrhosis andportal hypertension) and end-stage kidney disease (eGFR< 30 ml/min), or terminalillness.
Subjects with a history of cognitive impairment, dementia, or mental conditionrendering the subject unable to understand the nature and consequences of the study
Study Design
Study Description
Connect with a study center
Grady Memorial Hospital
Atlanta, Georgia 30303
United StatesSite Not Available
Grady Memorial Hospital
Atlanta 4180439, Georgia 4197000 30303
United StatesActive - Recruiting

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