| Trial ID: | L0549 |
| Source ID: | IRCT201701162709N39
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| Associated Drug: |
Sumac
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| Title: |
The effect of supplementation with sumac powder on liver enzymes (Alanine aminotransferase and Aspartate aminotransferase ), lipid profiles(Triglyceride,Total cholestrol,High density lipoprotein,Low density lipoprotein)? leptin and liver steatosis in pat
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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: |
Nonalcoholic fatty liver. <br>Fatty (change of) liver, not elsewhere classified;Fatty (change of) liver, not elsewhere classified
|
| Interventions: |
Intervention 1: Control group: daily 2 g dextrin as 4 capsules of 500 mg. Intervention 2: Intervention group: daily 2 g sumac as 4 capsules of 500 mg.;Treatment - Drugs;Treatment - Drugs;Control group: daily 2 g dextrin as 4 capsules of 500 mg;Interventio
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| Outcome Measures: |
Alanine aminotransferase. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Spectrophotometry.;Aspartate aminotransferase. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Spectrophotometry.;Hepatic steatosis. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Using the scanning fiber 502.Total cholestrol. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Spectrophotometry.;Triglycerides. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Spectrophotometry.;Low density lipoprotein. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Spectrophotometry.;High density lipoprotein. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Spectrophotometry.;Leptin. Timepoint: Before the start of treatment and 12 weeks after intervention. Method of measurement: Elisa.
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| Sponsor/Collaborators: |
Vice Chancellor for Research of Iran university Medical Sciences
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| Gender: |
All
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| Age: |
20 years60 years
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| Phases: |
Not applicable
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| Enrollment: |
80
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| Study Type: |
interventional
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| Study Designs: |
Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Supportive.
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| Start Date: |
06/05/2017
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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/2550
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