Clinical Trial Details

Trial ID: L0892
Source ID: IRCT2014090210826N14
Associated Drug: Purslane seeds
Title: Effect of Purslane seeds on liver enzymes, lipid profile and FBS in patients with nonalcoholic fatty liver disease
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Non alcoholic fatty liver. <br>Nonalcoholic fatty liver disease (NAFLD)
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
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.
Sponsor/Collaborators: Research deputy, Shahid Sadoughi University of Medical Sciences
Gender: All
Age: 25 years75 years
Phases: Phase 3
Enrollment: 60
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: computerized genererated random number table.
Start Date: 26/09/2014
Completion Date: --
Results First Posted: --
Last Update Posted: 14 January 2019
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/11246