Type 2 diabetes
Conditions
Interventions
ipraglifrozin 50mg/day for 24 weeks
Sponsors
St. Marianna University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Outpatients HbA1c >= 6.5% 20 <= BMI <= 40
Exclusion criteria
Exclusion criteria: The exclusion criteria were pregnancy, severe illness, CKD (eGFR < 60 ml/min/1.73m2), and malignancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| %Change of visceral fat volume assessed by CT and %change of intrahepatic lipid content assessed by 1H-MRS at 0-, 12- and 24-week of ipraglifrozin treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| beta-cell stress assessed by the change of plasma intact proinsulin / C-peptide (PI/CPR) ratio at 0-, 12- and 24-week of ipraglifrozin treatment | — |
Countries
Japan
Contacts
Public ContactYoshio Nagai
St. Marianna University School of Medicine Division of Metabolism and Endocrinology, Department of Internal Medicine
Outcome results
None listed