Trial ID: | L0840 |
Source ID: | IRCT2016080614882N4
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Associated Drug: |
Silymarin
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Title: |
Evaluation of sylimarin effect on non alcoholic fatty liver on children and adolescents
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Acronym: |
--
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Status: |
Not Recruiting
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Study Results: |
No Results Available
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Results: |
--
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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)
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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
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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.
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Sponsor/Collaborators: |
Vice Chancellor for Research of Shahrekord University of Medical Science
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Gender: |
All
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Age: |
5 years16 years
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Phases: |
Not applicable
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Enrollment: |
16
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Study Type: |
interventional
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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.
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Start Date: |
17/09/2016
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Completion Date: |
--
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Results First Posted: |
--
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Last Update Posted: |
22 February 2018
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Locations: |
Iran (Islamic Republic of)
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URL: |
http://en.irct.ir/trial/14348
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