type 2 diabetes
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients who are 65-year-old or older 2) Patients with HbA1c of 7.0% or higher 3) Patients who do not refuse to participate in this study
Exclusion criteria
Exclusion criteria: 1) Patients with a history of hypersensitivity to the components of semaglutide 2) Patients with severe ketosis, diabetic coma or pre-coma 3) Other patients deemed to be unsuitable by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The change from baseline in HbA1c after 6 months of treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) The change of various parameters in blood and urine tests (liver, kidney, lipid, etc.) 2) The changes of weight, abdominal circumference, blood pressure, and pulse rate. 3) Adverse events during observation period 4) Factors contributed to changes in HbA1c and secondary endpoints 5) The change of each factor when the degree of dementia is stratified by the simple cognitive function tests 6) Association between scores of simple cognitive function tests and the change of HbA1c | — |
Countries
Japan
Contacts
Hokkaido University Graduate School Department of Rheumatology, Endocrinology and Nephrology