type 2 diabetes
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients with written informed consent. 2) Aged over 30 years and under 80 years. 4) Type of practice: outpatient department. 5) Patients who will keep the rules to intake and to visit hospital.
Exclusion criteria
Exclusion criteria: 1) Patients who did not agree with joining this study. 2)Patients with severe renal dysfunction or severe hepatic dysfunction. 3)Pregnant women, women who may be pregnant, and breast-feeding women. 4)Patients treated with insulin. 5)Patients who are ineligible for some other reason judged by attending physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in HOMA-IR after 8 weeks of treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in FPG,HbA1c,total cholesterol, HDL,LDL,triglyceride,serum insulin,remnant like particle cholesterol(RLP-C),HMW-adiponectin,TNF-alpha,high sensitive CRP,IL-6 and urine pH after 8 weeks of treatment. | — |
Countries
Japan