Clinical Trial Details

Trial ID: L0521
Source ID: IRCT2017102537007N1
Associated Drug: Probiotic
Title: Effect of probiotic in improving laboratory findings in nonalcoholic fatty liver disease
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: In intervention group, two Gerilact tablets 500 mg will be administered daily for 60 days. Intervention 2: In control group, two placebo tablets will be given daily for 60 days.;Treatment - Drugs;Placebo;In intervention group, two Gerilact
Outcome Measures: Lipid profile. Timepoint: Before and at the end of intervention. Method of measurement: with laboratory examination.;Liver function tests. Timepoint: Before and at the end of intervention. Method of measurement: with laboratory examination.;Fatty liver grade. Timepoint: Before and at the end of intervention. Method of measurement: With sonography.nan
Sponsor/Collaborators: Vice chancellor for research, Ardabil University of Medical Sciences
Gender: All
Age: 18 yearsno limit
Phases: Not applicable
Enrollment: 60
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Triple blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
Start Date: 12/11/2017
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/27500