Type 2 diabetes mellitus
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Male and female subjects with type 2 Diabetes Mellitus 2.Age ≥20 years 3.Treated with stable dose of liraglutide of 0.6mg or 0.9mg for at least 2 weeks. 4.GA 30% or less 5.Able to provide informed consent before any trial-related activities.
Exclusion criteria
Exclusion criteria: 1-Type 1 Diabetes Mellitus 2-Previous treatment with other incretin mimetics within the previous three months before screening. 3-Insulin-requiring type 2 Diabetes Mellitus 4-Impaired hepatic function, measured as serum glutamic oxaloacetic transaminase [sGOT ( Aspartate Aminotransferase , ASAT)] or serum glutamic pyruvic transaminase (sGPT) ≥ 100 IU/L 5-Unstable cardiovascular or cerebrovascular disease. 6-Pregnant, breast-feeding or the intention of becoming pregnant or not using adequate contraceptive measures. 7-Female of childbearing potential who are not using adequate contraceptive menthods 8-Known or suspected allergy to trial medication(s), excipients, or related products. 9-Any contraindications to liraglutide.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plasma glucose profile (CGM) on-haemodialysis and off-haemodialysis | — |
Secondary
| Measure | Time frame |
|---|---|
| Plasma liragutide levels while on-haemodialysis and off-haemodialysis | — |
Countries
Japan
Contacts
Nakakinen Clinic Director