Trial ID: | L0708 |
Source ID: | IRCT20191009045043N1
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Associated Drug: |
Sumac
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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
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Acronym: |
--
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Status: |
Recruiting
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Study Results: |
No Results Available
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Results: |
--
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Conditions: |
Nonalcoholic Fatty Liver Disease. <br>Liver disorders in diseases classified elsewhere
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Interventions: |
Intervention 1: Intervention group: Sumac powder capsule + diet. Intervention 2: Control group: Medicinal starch capsule + diet.
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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
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Sponsor/Collaborators: |
Shiraz University of Medical Sciences
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Gender: |
All
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Age: |
20 years60 years
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Phases: |
Phase 2/Phase 3
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Enrollment: |
46
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Study Type: |
interventional
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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
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Start Date: |
20/01/2020
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Completion Date: |
--
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Results First Posted: |
--
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Last Update Posted: |
24 February 2020
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Locations: |
Iran (Islamic Republic of)
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URL: |
http://en.irct.ir/trial/43090
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