Effect of Nigella sativa seed oil in treatment of non-alcoholic fatty liver disease
Not Applicable
- Conditions
- on-alcoholic fatty liver disease.Fatty (change of) liver, not elsewhere classified
- Registration Number
- IRCT20090804002288N13
- Lead Sponsor
- Iranian academic center for education culture and research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Patients whose hepatic sonography shows they have fatty liver disease
Age of 20 to 70 years
Exclusion Criteria
Child-Pugh score above 7
Hepatic disease other than non-alcoholic fatty liver disease
Pregnant women
Women planning pregnancy
Lactating women
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fatty liver grade. Timepoint: Before intervention and 3 month? after intervention. Method of measurement: Liver sonography.;Blood level of ALT. Timepoint: Before intervention and 3 months after intervention. Method of measurement: Medical laboratory (kit).;Blood level of AST. Timepoint: Before intervention and 3 months after intervention. Method of measurement: Medical laboratory (kit).;Blood level of LDL-C. Timepoint: Before intervention and 3 months after intervention. Method of measurement: Medical laboratory (kit).;Blood level of triglyceride. Timepoint: Before intervention and 3 months after intervention. Method of measurement: Medical laboratory (kit).
- Secondary Outcome Measures
Name Time Method Blood level of HDL-C. Timepoint: Before intervention and 3 month after intervention. Method of measurement: Medical laboratory (kit).