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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
NameTimeMethod
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
NameTimeMethod
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.
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