Clinical Trial Details

Trial ID: L0614
Source ID: IRCT2015012520781N1
Associated Drug: Silymarin
Title: Evaluation of the effect of silimarin in children with nonalcoholic fatty liver disease
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic fatty liver disease. <br>Fatty (change of) liver, not elsewhere classified;Fatty (change of) liver, not elsewhere classified
Interventions: Intervention 1: In the case group Silimarin capsule manufactured by Sabz Daroo company with dose of 140 mg three times a day is used for 3 months. Intervention 2: In the control group placebo capsule filled with starch, made by the researcher is used t
Outcome Measures: AST. Timepoint: Before and after the treatment. Method of measurement: mg/dL.;ALT. Timepoint: Before and after the treatment. Method of measurement: mg/dL.;Fatty liver disease stage. Timepoint: Before and after the treatment. Method of measurement: Ultrasonography.;TG. Timepoint: Before and after the treatment. Method of measurement: mg/dL.;HDL. Timepoint: Before and after the treatment. Method of measurement: mg/dL.;LDL. Timepoint: Before and after the treatment. Method of measurement: mg/dL.nan
Sponsor/Collaborators: Qom University of Medical Sciences
Gender: All
Age: 5 years16 years
Phases: Not applicable
Enrollment: 40
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Crossover, Purpose: Treatment.
Start Date: 04/04/2015
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/18376