Clinical Trial Details

Trial ID: L0840
Source ID: IRCT2016080614882N4
Associated Drug: Silymarin
Title: Evaluation of sylimarin effect on non alcoholic fatty liver on children and adolescents
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: non alcoholic fatty liver disease. <br>Fatty (change of) liver, not elsewhere classified Nonalcoholic fatty liver disease (NAFLD);Fatty (change of) liver, not elsewhere classified Nonalcoholic fatty liver disease (NAFLD)
Interventions: Intervention 1: intervention group : Livergol tablet containing silymarin(Goldaru Company, Iran) were administered for 12 weeks with dosage of 5 mg per kg body weight divided in three dose with meal. Patients are visited weight, height and compliance
Outcome Measures: Grading of fatty liver in sonography. Timepoint: At arrival to study and 12 weeks later. Method of measurement: Sonographic grading.Liver enzymes, transaminases. Timepoint: At arrival and after 12 weeks. Method of measurement: Serum.
Sponsor/Collaborators: Vice Chancellor for Research of Shahrekord University of Medical Science
Gender: All
Age: 5 years16 years
Phases: Not applicable
Enrollment: 16
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: Randomization was done base of random table number.
Start Date: 17/09/2016
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/14348