Clinical Trial Details

Trial ID: L0635
Source ID: IRCT201301223140N6
Associated Drug: Probiotic
Title: The effects of probiotic, prebiotic and concomitant supplementation of probiotic, Prebiotic on the oxidative stress, inflammatory and insulin resistance indices, lipid profile and liver function in non-alcoholic fatty liver. patients.
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Non alcoholic fatty liver. <br>Other diseases of liver;Other diseases of liver
Interventions: Intervention 1: Intervention groups: Group1 treated with 1 gr of probiotic capcul (107 Bifidobacterium longum and Lactobacillus acidophilus) and 5 gr of prebiotic plasebo (multodextrose) twice a day for 3 months. Group 2 treated with 5 gr of prebiotic (in
Outcome Measures: AST. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;ALT. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;?GT. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;ALP. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;ALB. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;BIL. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;TC. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;TG. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;LDL. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;HDL. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;Hs-CRP. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;TNF-a. Timepoint: Befor and after intervention. Method of measurement: Serum of blood,ELISA.;IL-6. Timepoint: Befor and after intervention. Method of measurement: Serum of blood,ELISA.;MDA. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;TAC. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;Insulin. Timepoint: Befor and after intervention. Method of measurement: Serum of blood,ELISA.;FBS. Timepoint: Befor and after intervention. Method of measurement: serum of blood, by outoanalyzer.;HOMA-IR. Timepoint: Befor and after intervention. Method of measurement: srrum insulin*FBS/405.Body mass index. Timepoint: Befor and after intervention. Method of measurement: W/H2.;WRT. Timepoint: Befor and after intervention. Method of measurement: waist to hip ratio.;Intake micro and macro nutrients. Timepoint: Befor and after intervention. Method of measurement: Three days weighing food questionnaires.
Sponsor/Collaborators: Vice-chancellor for research-Tabriz University of Medical Science
Gender: All
Age: 20 years60 years
Phases: Phase 2
Enrollment: 88
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
Start Date: 16/01/2014
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/3178