Effect of squill oxymel in control of mild to moderate fatty liver
- Conditions
- fatty liver.k75.8
- Registration Number
- IRCT201705261165N20
- Lead Sponsor
- Vice chancellor for research Baqiyatallah University of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
To Sign the consent form Knowingly
patients be suffered from mild to moderate fatty liver According to the ultrasound result.
Exclusion criteria:
Off treatment for more than a week
Progression of Fatty liver disease
Person is pregnant or lactating
Allergic reactions to herbal blend
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvment of quality of life. Timepoint: at baseline and 2 month after intervention. Method of measurement: quality of life questionnaire.;FBS. Timepoint: at baseline and 2 month after intervention. Method of measurement: mg/dl.;Triglycerides. Timepoint: at baseline and 2 month after intervention. Method of measurement: mg/dl.;Cholesterol. Timepoint: at baseline and 2 month after intervention. Method of measurement: mg/dl.;Hdl. Timepoint: at baseline and 2 month after intervention. Method of measurement: mg/dl.;Ldl. Timepoint: at baseline and 2 month after intervention. Method of measurement: mg/dl.;Alt. Timepoint: at baseline and 2 month after intervention. Method of measurement: iu/l.;Ast. Timepoint: at baseline and 2 month after intervention. Method of measurement: iu/l.;Alp. Timepoint: at baseline and 2 month after intervention. Method of measurement: iu/l.;Grade of fatty liver. Timepoint: at baseline and 2 month after intervention. Method of measurement: sonography.
- Secondary Outcome Measures
Name Time Method Bmi. Timepoint: at baseline and 2 month after intervention. Method of measurement: kg/m2.
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