diabetes mellitus
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients with type 2 diabetes with HbA1c=> 7% at the time of consenting 2.Female and male patients over 20 years old 3.Patients have been taking daily linagliptin for more than 12 weeks 4.Patients who can provide their written consent for participation of this study
Exclusion criteria
Exclusion criteria: 1.Patients with history of hypersensitivity to teneligliptin 2.Patients with diabetic ketoacidosis, diabetic coma, or bofore coma, type1 diabetes 3.Severe infection, before and not long after surgery, or patient with severe trauma 4.Women with during pregnancy , nursing, or pregnant likelihood 5.Patients with severe renal dysfunction ,end stage renal disease during dialysis 6.Patients with severe liver dysfunction 7.Inadequte patient judged by doctor
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Amount of change in HbA1c after administration 24 weeks later | — |
Secondary
| Measure | Time frame |
|---|---|
| Casual blood glucose, glycoalbumin Serum lipid level(total cholesterol, LDL-cholesterol, triglyceride, HDL-cholesterol) Urinary albumin, urinary L-FABP The incidence of side effects | — |
Countries
Japan
Contacts
Juntendo University Urayasu Hospital Endocrinology and Diabetology