To evaluate the efficacy of once-weekly DPP-4 inhibitor:Omarigliptin for liver function of type 2 diabetic patients with NAFLD/NASH
Not Applicable
- Conditions
- Type 2 diabetes
- Registration Number
- JPRN-UMIN000045957
- Lead Sponsor
- Department of Diabetes and Metabolism,Tohto Clinic
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 26
Inclusion Criteria
Not provided
Exclusion Criteria
1)Pregnant or being pregnant within the study 2)Contraindication with Dipeptidyl peptidase 4 inhibitor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fasting blood glucose,HbA1c and liver function are set to be measured at baseline and once at 3 months for 36 months. Abdominal ultrasonography is set to be examined at baseline and once at 6 months for 36 months.
- Secondary Outcome Measures
Name Time Method Body mass index(BMI),body pressure,immunoreactive insulin(IRI),homeostasis model assessment for insulin resistance(HOMA-IR),high-sensitivity C-reactive protein(hsCRP) and lipid function are set to be measured at baseline and once at 3 months for 36 months.