Clinical Trial Details

Trial ID: L0541
Source ID: IRCT2017060212789N14
Associated Drug: Rosvastatin
Title: The effect of Rosvastatin on steatosis and fibrosis in patients with non-alcoholic fatty liver disease: a randomized controlled clinical trial study
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic fatty liver disease (NAFLD). <br>Fatty (change of) liver, not elsewhere classified;Fatty (change of) liver, not elsewhere classified
Interventions: Intervention 1: Control Group: patients received placebo daily plus standard treatment for fatty liver disease. Intervention 2: Intervention Group: patients received 10 mg Rosvastatin daily plus standard treatment for fatty liver disease.;Treatment - Drug
Outcome Measures: 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.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.
Sponsor/Collaborators: Vice Chancellor for Research of Kurdistan University of Medical Sciences
Gender: All
Age: 20 years70 years
Phases: Phase 3
Enrollment: 40
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
Start Date: 12/06/2017
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/12802