NAFLD Clinical Trial
Official title:
Efficacy and Tolerability of Vitamin D and Docosahexaenoic Acid (DHA) in Children With Biopsy Proven NAFLD
Non-alcoholic fatty liver disease (NAFLD) has reached epidemic proportions and is rapidly
becoming the one of most common causes of chronic liver disease in children. The
pathogenesis of NAFLD is generally considered the result of a series of liver injuries,
commonly referred as "multi-hit" hypothesis. Several studies suggest that inflammatory
pathways and oxidative stress could be responsible of disease progression.
The purpose of this interventional study is to evaluate the efficacy and tolerability of
docosahexaenoic acid (DHA) and Vitamin D in children and adolescents with biopsy-proven
nonalcoholic fatty liver disease (NAFLD).
Sixty-six children or adolescents (4-16 years) with liver biopsy proven NAFLD will be
enrolled. They will be randomized to treatment with DHA and Vitamin D (n=33) or an identical
placebo (n=33) given orally for a period of 6 months. All patients will be included in a
lifestyle intervention program consisting of a diet tailored on the individual requirements
and physical exercise.
Patients will undergo a medical evaluation at 3-6 and 12 months during the 12-months study
period. Liver biopsy will be performed at baseline and at 12 months. Anthropometric
measurements and laboratory tests, including liver enzymes, gluco-insulinemic profile and
lipids will be performed at baseline and repeated at 6-12 months
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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