Clinical Trial Details

Trial ID: L0583
Source ID: IRCT2016040727265N1
Associated Drug: Ursobil
Title: Comparison of the effect of Ursobil and Silymarine in non alchoholic fatty liver
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic steatohepatitis. <br>nonalcoholic steatohepatitis;nonalcoholic steatohepatitis
Interventions: Intervention 1: First group will be received Ursobil (oral capsule; 300mg BD for 4 weeks). Intervention 2: Second group will be received Silymarin (oral tablet ; 140 mg BD for 4 weeks).;Treatment - Drugs;Treatment - Drugs;First group will be received Ur
Outcome Measures: Liver enzymes. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: By laboratory analysis ( blood test).;Serum insulin. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Chemiluminescence.;Fasting blood sugar. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: By laboratory analysis ( blood test).;Lipid profile. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: By laboratory analysis ( blood test).;Inflammatory marker. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: By laboratory analysis ( blood test).nan
Sponsor/Collaborators: Vice Chancellor for research Qazvin University of Medical Sciences
Gender: All
Age: no limitno limit
Phases: Phase 3
Enrollment: 70
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.
Start Date: 29/05/2016
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of);Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/22380