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The effect of Rosvastatin on steatosis and fibrosis in patients with non-alcoholic fatty liver disease

Phase 3
Conditions
onalcoholic fatty liver disease (NAFLD).
Fatty (change of) liver, not elsewhere classified
Registration Number
IRCT2017060212789N14
Lead Sponsor
Vice Chancellor for Research of Kurdistan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Main Inclusion Criteria: Non diabetics patients; normal FBS; BS2hpp;Hb1AC; Age 20 years and older; approved non fatty liver diagnosed by fibroscan; LFT(AST and ALT); rejection of other causes of fatty liver disease such as hepatitis B and C .
Main

Exclusion Criteria

Patients who have other liver diseases; contraindication for Rosvastatin; not taking hypoglycemic drugs such as metformin.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Steatosis of liver. Timepoint: Before intervention, six month after intervention. Method of measurement: Fibroscan.;Fibrosis of liver. Timepoint: Before intervention, six month after intervention. Method of measurement: Fibroscan.
Secondary Outcome Measures
NameTimeMethod
ALT. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;AST. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;LDL. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;HDL. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Triglyceride. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Bilirubin. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Blood urea. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Blood creatinine. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.
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