Clinical Trial Details

Trial ID: L0899
Source ID: IRCT2014020516491N1
Associated Drug: CLA
Title: The effect of conjugated linoleic acid(CLA) on insulin resitsance, lipid profile, oxidative stress, inflammatory factors and resistin in obese patients with Non-alcoholic fatty liver disease (NAFLD) under weight loss diet :A randomized clinical control tr
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: non- alcoholic fatty liver disease. <br>Fatty (change of) liver, not elsewhere classified;Fatty (change of) liver, not elsewhere classified
Interventions: Intervention 1: 3 caposouls of CLA(each containing 1000mg, daily 3000mg) with weight loss diet for eight weeks in intervention group. Intervention 2: weight loss diet for eight weks in control group.;Treatment - Drugs;Treatment - Other;3 caposouls of CLA(
Outcome Measures: Resistin. Timepoint: Beginning and end of the intervention. Method of measurement: Elisa.;Inflammatory factors(IL-6,Il-10,TNFa,hs-CRP). Timepoint: Begining and end of the study. Method of measurement: IL-6,Il-10,TNFa: Elisa and hs-CRP : immunoturbidimetry.;Insulin resistance and Insulin sensitivity. Timepoint: Beginning and end of the intervention. Method of measurement: Insulin resistance with HOMA-IR index and Insulin sensitivity with Quicki index.;Liver enzymes(AST-ALT-ALP). Timepoint: Beginning and end of the intervention. Method of measurement: IFCC.;Lipid profile. Timepoint: Beginning and end of the intervention. Method of measurement: Spectrophotometry and Friedewald Formula for LDL.;Oxidative Stress Indicies(TAC-ARE-MDA). Timepoint: Beginning and end of the intervention. Method of measurement: TAC and ARE : spectrophotometry and MDA : thiobarbituric acid.;?Sonography faindings. Timepoint: Beginning and end of the intervention. Method of measurement: Liver Sonography.Anthropometry(BMI-WC-WHR-WHtR). Timepoint: Beginning, second, fourth, sixth and end of the intervention. Method of measurement: metr, scale and stadiometr.;Body composition. Timepoint: Beginning and end of the intervention. Method of measurement: BIA.;Energy and nutrient intake. Timepoint: beginning, fourth week and end of the intervention. Method of measurement: 3 day food record.;Comparison of physical activity. Timepoint: beginning, fourth week and end of the intervention. Method of measurement: Physical Activity Questionnaire.
Sponsor/Collaborators: Deputy of research, Tabriz University of Medical Sciences
Gender: All
Age: 20 years50 years
Phases: Not applicable
Enrollment: 46
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.
Start Date: 09/06/2014
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/15422