type 2 diabetes
Conditions
Interventions
Sponsors
Kyoto Prefectural University of Medicine, Graduate School of Medical Science
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients who are able to give written informed consent 2) Age is over 35 years and less than 75 years 3) Type of practice: outpatient department 4) Patients are able to do the following things in this trial - getting good compliance with consuming investigational food and coming to hospital
Exclusion criteria
Exclusion criteria: 1) Patients who did not agree with this study 2)Patients with severe renal dysfunction and severe hepatic dysfunction 3)Pregnant women, women who may be pregnant, and breast-feeding women 4)Patients treated with insulin 5)Patients judged by the investigator to be ineligible for some other reason
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CO2 output, urine pH, HOMA-IR | — |
Secondary
| Measure | Time frame |
|---|---|
| fasting plasma glucose, HbA1c, serum insulin, blood ketone body, total cholesterol, HDL. LDL, triglyceride, remnant lile particle cholesterol(RLP-C), uric acid | — |
Countries
Japan
Contacts
Public ContactTakuya Fukuda
Kyoto Prefectural University of Medicine, Graduate School of Medical Science Department of Endocrinology and Metabolism
Outcome results
None listed