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October 30, 2017 summary This study aimed to investigate the effect of calcitriol treatment on non-alcoholic fatty liver disease (NAFLD) patients with different genetic polymorphisms of vitamin D receptor. In a single center randomized double-blind placebo controlled trial; 160 participants aged between 18 and 60 years with hepatic steatosis are treated with Calcitriol (25 µg/day) for 16 weeks. Patients are randomized to receive calcitriol or placebo. Major inclusion criteria include: men and women aged between 18 and 60 years with presence of hepatic steatosis diagnosed by Fibroscan elastography and increased liver enzymes. Major exclusion criteria include: patients with chronic liver diseases, alcohol consumption, hypercalcemia and those receiving hepatotoxic drugs. Intervention: Calcitriol and placebo for 16 weeks. The primary outcome: improvement in serum ALT, AST, GGT. Secondary outcomes are improvement of hepatic steatosis and metabolic component of patients including fasting plasma glucose, LDL, HDL, triglyceride and total cholesterol.
October 30, 2017 Intervention/Control 1 25 µg/day calcitriol for 16 weeks
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