Clinical Trial Details

Trial ID: L0708
Source ID: IRCT20191009045043N1
Associated Drug: Sumac
Title: Investigation the effect of the Sumac powder on Liver Enzymes, lipid profile, glycemic indexes, Antioxidant marker, inflammatory marker, anthropometric measurements in non-alcoholic fatty liver patients with overweight or obes
Acronym: --
Status: Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic Fatty Liver Disease. <br>Liver disorders in diseases classified elsewhere
Interventions: Intervention 1: Intervention group: Sumac powder capsule + diet. Intervention 2: Control group: Medicinal starch capsule + diet.
Outcome Measures: Alanine aminotransferase (ALT) enzyme. Timepoint: Baseline and the end of the intervention. Method of measurement: ALT kit.;Aspartate aminotransferase (AST) enzyme. Timepoint: Baseline and the end of the intervention. Method of measurement: AST kit.;Weight. Timepoint: Baseline and the end of the intervention. Method of measurement: scale/ kg.;Cholestrol. Timepoint: Baseline and the end of the intervention. Method of measurement: Cholestrol Kit.;Triglyceride. Timepoint: Baseline and the end of the intervention. Method of measurement: Triglyceride Kit.;Low-density lipoprotein. Timepoint: Baseline and the end of the intervention. Method of measurement: Low-density lipoprotein Kit.;High-density lipoprotein. Timepoint: Baseline and the end of the intervention. Method of measurement: High-density lipoprotein Kit.;Fasting blood suger. Timepoint: Baseline and the end of the intervention. Method of measurement: Fasting blood suger Kit.;Insulin. Timepoint: Baseline and the end of the intervention. Method of measurement: Insulin Kit.;Total Antioxidant Capacity. Timepoint: Baseline and the end of the intervention. Method of measurement: Total Antioxidant Capacity Kit.;Tumor Necrosis Factor alpha. Timepoint: Baseline and the end of the intervention. Method of measurement: Tumor Necrosis Factor alpha Kit.;Alkaline Phosphatase. Timepoint: Baseline and the end of the intervention. Method of measurement: Alkaline Phosphatase kit.;Height. Timepoint: Baseline and the end of the intervention. Method of measurement: Meter.;Waist circumference. Timepoint: Baseline and the end of the intervention. Method of measurement: Meter.;Hip circumference. Timepoint: Baseline and the end of the intervention. Method of measurement: Meter.;Fat mass. Timepoint: Baseline and the end of the intervention. Method of measurement: BIA device.;Fat Free mass. Timepoint: Baseline and the end of the intervention. Method of measurement: BIA device.;Total Body Water. Timepoint: Baseline and the end of the intervention. Method of measurement: BIA device.;Body cell mass. Timepoint: Baseline and the end of the intervention. Method of measurement: BIA device.;Gama glutamil transferase enzyme. Timepoint: Baseline and the end of the intervention. Method of measurement: gama glutamil transferase KIt.nan
Sponsor/Collaborators: Shiraz University of Medical Sciences
Gender: All
Age: 20 years60 years
Phases: Phase 2/Phase 3
Enrollment: 46
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment, Randomization description: Based on block randomization and 4 blocks, the entry of patients into the two study groups will be randomized by using
Start Date: 20/01/2020
Completion Date: --
Results First Posted: --
Last Update Posted: 24 February 2020
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/43090