Clinical Trial Details

Trial ID: L0645
Source ID: IRCT201202014010N7
Associated Drug: Resveratrol
Title: Evaluating the effect of Resveratrol supplement on lipid profile, hepatic enzymes, inflammatory factors, and hepatic fibrosis in patients with Nonalcoholic Fatty Liver Disease (NAFLD)
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Non Alcoholic Fatty Liver. <br>Inflammatory liver disease, unspecified;Inflammatory liver disease, unspecified
Interventions: Intervention 1: Intervention: Soft gel Resveratrol 500 mg once a day /12 weeks. Intervention 2: Placebo: Edible paraffin soft gelonce a day/ 12 weeks.;Treatment - Drugs;Placebo;Intervention: Soft gel Resveratrol 500 mg once a day /12 weeks;Placebo: Edible
Outcome Measures: Liver Enzymes. Timepoint: at the first and at the 12th week of the study. Method of measurement: Biochemical analysis.Liver fibrosis. Timepoint: at the first and the end of the study. Method of measurement: Fibroscan.
Sponsor/Collaborators: National Nutrition and Food Technology Research Institute
Gender: All
Age: 18 years65 years
Phases: Phase 2/Phase 3
Enrollment: 50
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
Start Date: 11/01/2013
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/4188