Type 2 diabetes
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Patients of type 2 diabetes with HbA1c>=7.0 2)Paitents over 20 years old and under 75 years old 3)Patients give written informed consent
Exclusion criteria
Exclusion criteria: 1) History of hypersensitivity of canagliflozin 2) Severe ketosis, diabetic coma or precoma 3) Severe infection, pre or post surgery, or severe trauma 4) Patients taking fibrate-based medicines or pioglitazone 5) Patients taking diuretic medicines 6) eGFR < 45 mL/min/1.73 m2 or artificial dialysis 7) Considered as inadequate by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of the data of 20 lipoproteins fractions measured by high-performance gel permeation chromatography at 3 months after canagliflozin administration | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Change of hemoglobin A1c (HbA1c) for 3 months at 3 months after canagliflozin administration 2) Change of body mass and body mass index (BMI) at 3 months after canagliflozin administration 3) Change of blood biochemical value at 3 months after canagliflozin administration | — |
Countries
Japan
Contacts
Tokyo Medical and Dental University Medical Genetics/ Geriatrics