Clinical Trial Details

Trial ID: L0523
Source ID: IRCT201703194010N18
Associated Drug: Citrulline
Title: The effect of citrulline supplementation on serum lipids, liver enzymes, inflammatory markers and hepatic steatosis in patient with nonalcoholic fatty liver disease
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: non alcoholic fatty liver disease. <br>Other specified inflammatory liver diseases;(K75.8);Other specified inflammatory liver diseases
Interventions: Intervention 1: intervention group:2 gram citrulline per day for three months. Intervention 2: placebo group:2 gram starche per day for three months.;Treatment - Other;intervention group:2 gram citrulline per day for three months;placebo group:2 gram st
Outcome Measures: LDL-C. Timepoint: Being andend of intervention. Method of measurement: Enzymatic methods using kits.;HDL-C. Timepoint: Being andend of intervention. Method of measurement: Enzymatic methods using kits.;TG. Timepoint: Being andend of intervention. Method of measurement: Enzymatic methods using kits.;Total Cholesterol. Timepoint: Being andend of intervention. Method of measurement: Enzymatic methods using kits.;FBS. Timepoint: Being andend of intervention. Method of measurement: Enzymatic methods using kits.;Fasting insulin. Timepoint: Being andend of intervention. Method of measurement: Radioimmunoassay ??U/mL.;AST. Timepoint: Being andend of intervention. Method of measurement: Enzymatic methods using kits.;ALT. Timepoint: Being andend of intervention. Method of measurement: Enzymatic methods using kits ??g/m.;HOMA. Timepoint: Being andend of intervention. Method of measurement: Calculation.;TNF-a. Timepoint: Being andend of intervention. Method of measurement: Elisa Pg/dl.;IL_6. Timepoint: Being andend of intervention. Method of measurement: Elisa Pg/dl.;Steatosis. Timepoint: Being andend of intervention. Method of measurement: Ultrasonography Grade 0: absence of steatosis grade 1: mild steatosis grade 2: moderate steatosis grade 3: severe steatosis.Total energy intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire Kcal per day.;Carbohydrate intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire gram per day.;Protein intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire gram per day.;Total fat intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire gram per day.;SAFA intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire gram per day.;PUFA intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire gram per day.;MUFA intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire gram per day.;Total fiber intake. Timepoint: Beginning and end of intervention. Method of measurement: questionnaire gram per day.
Sponsor/Collaborators: Shahid Beheshti University of Medical Sciences, National Nutrition and Food Technology Research
Gender: All
Age: no limitno limit
Phases: Not applicable
Enrollment: 50
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Single blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
Start Date: 13/10/2017
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/4196