This study aims to evaluate the possible beneficial effect of empagliflozin versus pioglitazone on non-diabetic patients with non-alcoholic steatohepatitis (NASH). This study will be a randomized, comparative parallel study. The study will be conducted according to the ethical standards of Helsinki declaration in 1964 and its later amendments. The study duration will be 24 weeks. The patients will be randomized into two groups: Group 1: (Pioglitazone group; n=28) which will receive 30mg/day pioglitazone for 24 weeks. Group 2: (Empagliflozin group; n=28) which will receive 10mg/day empagliflozin for 24 weeks.
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Change in fibrosis index based on the 4 factors (FIB-4)
Timeframe: Baseline and 24th week
Change in aspartate transaminase-to-platelet ratio index (APRI)
Timeframe: Baseline and 24th week
Change in liver enzymes
Timeframe: Baseline, 12th and 24th week