type 2 diabetes mellitus
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All subjects presented with postprandial hyperglycemia in spite of administration of alogliptin (25mg) for more than 1 week. Participants provided their informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: Patients using insulin therapy, those who were or may have been pregnant, and those with severe liver dysfunction (AST and ALT: 3 times the normal levels) were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure used was SD of glucose and this was compared between the alpha-GIs (both being used in combination with alogliptin) | — |
Countries
Japan
Contacts
University of Occupational and Environmental Health First Department of Internal Medicine, School of Medicine