Trial ID: | L0892 |
Source ID: | IRCT2014090210826N14
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Associated Drug: |
Purslane seeds
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Title: |
Effect of Purslane seeds on liver enzymes, lipid profile and FBS in patients with nonalcoholic fatty liver disease
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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: |
Non alcoholic fatty liver. <br>Nonalcoholic fatty liver disease (NAFLD)
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Interventions: |
Intervention 1: Intervention group: using low caloric diet (kilo caloric/ body weight) - 500.15% protein, 55% carbohydrate, 30% fat.also they use10 gr purslane seed daily for 8 weeks. Intervention 2: Control group: using low caloric diet (kilo caloric/ bo
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Outcome Measures: |
Liver supersonic graphy. Timepoint: before & after intervention. Method of measurement: radiologic picture.;AST. Timepoint: before and after intervention. Method of measurement: blood sample.;ALT. Timepoint: before and after intervention. Method of measurement: blood sample.;Alkalin phosphat. Timepoint: before and after intervention. Method of measurement: blood sample.Triglycerid. Timepoint: before and after intervention. Method of measurement: mgr/dl, blood sample.;Insulin. Timepoint: before and after intervention. Method of measurement: blood sample.;Malon di aldehid. Timepoint: before and after intervention. Method of measurement: blood sample.;DPPH. Timepoint: before and after intervention. Method of measurement: blood sample.;Weight. Timepoint: before avd after intervention. Method of measurement: digital scale.;Hieght. Timepoint: before avd after intervention. Method of measurement: stadiometer,m.;Waist circumfrence. Timepoint: before avd after intervention. Method of measurement: meter,cm.;FBS. Timepoint: before and after intervention. Method of measurement: mg/dl.;Total cholestrol. Timepoint: before and after intervention. Method of measurement: mgr/dl, blood sample.;LDL. Timepoint: before and after intervention. Method of measurement: mgr/dl, blood sample.;HDL. Timepoint: before and after intervention. Method of measurement: mgr/dl, blood sample.
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Sponsor/Collaborators: |
Research deputy, Shahid Sadoughi University of Medical Sciences
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Gender: |
All
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Age: |
25 years75 years
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Phases: |
Phase 3
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Enrollment: |
60
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Study Type: |
interventional
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Study Designs: |
Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: computerized genererated random number table.
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Start Date: |
26/09/2014
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Completion Date: |
--
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Results First Posted: |
--
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Last Update Posted: |
14 January 2019
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Locations: |
Iran (Islamic Republic of)
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URL: |
http://en.irct.ir/trial/11246
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