Clinical Trial Details

Trial ID: L0662
Source ID: IRCT201109197590N1
Associated Drug: Ezetimibe
Title: Comparison the effect of ezetimibe and acarbose on biochemical indices in patient with nonalcoholic fatty liver disease
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: non alcoholic fatty liver disease. <br>Fatty (change of) liver;Fatty (change of) liver
Interventions: Intervention 1: 50 mg acarbose 3 times per day, oral, in acarbose group. Intervention 2: 10 mg ezetimibe once per day, oral, in ezetimibe group.;Treatment - Drugs;Treatment - Drugs;50 mg acarbose 3 times per day, oral, in acarbose group;10 mg ezetimibe on
Outcome Measures: Liver enzyme, AST, aspartate aminotransferase. Timepoint: Before and 2 months after treatment. Method of measurement: Lab kit.;Liver enzyme, ALT, alanine aminotransferase. Timepoint: Before and 2 months after treatment. Method of measurement: Lab kit.Insulin resistance index. Timepoint: Before and 2months after treatment. Method of measurement: Fasting glycemia mmol/L?? fasting insulinemiaMIU/L/22 .lab kit.;Inflamation index hs CRP. Timepoint: Before and 2 months after treatment. Method of measurement: Lab kit.
Sponsor/Collaborators: Vice chancellor for research, Qazvin University of Medical Sciences
Gender: All
Age: 18 yearsno limit
Phases: Phase 2
Enrollment: 31
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.
Start Date: 23/12/2011
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/8080