Type 1 diabetes
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The inclusion criteria were a diagnosis of type 1 diabetes and treatment with the MiniMed 770G system.
Exclusion criteria
Exclusion criteria: Patients for whom participation in this study is difficult due to concomitant severe liver disease. Patients deemed inappropriate for participation by the principal investigator or subinvestigators for any other reason.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in average blood glucose from baseline 12 weeks after switching to 780G | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes at 4 weeks, 12 weeks, and 24 weeks from the start of the study Weight, waist circumference, BMI Blood pressure, pulse rate Other blood and urine tests Daily blood glucose variability indices by treatment 24-hour average blood glucose Percentage of time in target range (TIR; time spent within 70-180 mg/dL) Length of time with blood glucose below 70 mg/dL (TBR; Percentage of time below target range) Length of time with blood glucose above 180 mg/dL (TAR; Percentage of time above target range) Daily blood glucose variability index Hourly blood glucose AUC, MAGE, SD, MODD Association with patient background and laboratory values affecting the above data Patient questionnaires related to diabetes treatment satisfaction and QOL Association with patient background and laboratory values affecting the above data Patient background and clinical laboratory values affecting the above data | — |
Countries
Japan
Contacts
Kushiro Red Cross Hospital Department of Internal Medicine