Type2 Diabetes
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with new onset or poorly controlled type 2 diabetes who are newly or additionally prescribed sitagliptin
Exclusion criteria
Exclusion criteria: 1.Patients sufferd from severe ketosis, diabetic coma or semi-coma within 6-month before participating the study 2.Patients sufferd from severe infection or trauma, and perioperative 3.Possible or definitive pregnant women or nursing mother 4.Serum creatine levels are 1.5mg/dL or more 5.Patients with history of hypersensitivity to any ingredients of sitagliptin tablets 6.Other patients deemed not appropliate for participating to the study by investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The change of HbA1c levels after prescribing sitagliptin | — |
Secondary
| Measure | Time frame |
|---|---|
| the incidence of cardio-, cerebro-vascular events or diabetes-related complications | — |
Countries
Japan
Contacts
Juntendo University School of Medicine Clinical Research Support Center