type 2 diabetes
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria were adequate endogenous insulin secretion (urinary C-peptide > 40 microgram/day) and controlled HbA1c levels of <= 7.5% on intensive insulin therapy with insulin dose of < 30 units.
Exclusion criteria
Exclusion criteria: 1, Subjects who have already been treated with oral hypoglycemic agents. 2, Subjects who are hypersensitive to this medicine and/or contaminants of this medicine. 3, Any condition that the investigator considers a potential obstacle to trial participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the parameters related to glucose profile of the subjects and proinsulin to C-peptide ratio before and after switching | — |
Secondary
| Measure | Time frame |
|---|---|
| Diabetes treatment satisfaction questionnaire (DTSQ), Frequency of side effects (digestive symptoms, hypoglycemia) | — |
Countries
Japan
Contacts
Kanto Rosai Hospital Department of Diabetes and Endocrinology