Polyunsaturated Fatty Acids (PUFA) in Diabetic Fatty Liver
Fatty Liver

About this trial
This is an interventional treatment trial for Fatty Liver focused on measuring PUFA, NASH, Fatty Liver, Insulin resistance, Metabolic syndrome, Nonalcoholic fatty liver disease, Nonalcoholic steatohepatitis, Type 2 Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria: Adult patients (age >18 years) Have type 2 diabetes mellitus with good control of blood sugar (hemoglobin A1c [HbA1c] <7.5%) and will have been on a stable regimen of anti-diabetic agents for more than 4 months. NASH established on liver biopsy done within 6 months prior to inclusion in the study as determined by established histologic criteria Exclusion Criteria: Cirrhosis of the liver End stage target organ damage in diabetes mellitus: advanced renal failure (serum creatinine > 2.0 mg/dl) with or without dialysis, severe neuropathy, or advanced peripheral vascular disease. Any organ dysfunction with anticipated life expectancy of less than 2 years Co-existent etiologies for liver disease Significant alcohol consumption, defined as more than 30 g per day in men and more than 20 g per day in women.
Sites / Locations
- MetroHealth Medical Center
- Cleveland Clinic Foundation
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Polyunsaturated fatty acid (Opti-EPA)
Placebo
Polyunsaturated fatty acid will consist of purified EPA:DHA (360 mg EPA and 240 mg DHA) 6 gelcaps-3 capsules by mouth 2x per day x 48 weeks
Gelcaps containing corn oil as placebo 6 capsules 3 capsules by mouth 2 x per day for 48 weeks