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Effect of squill oxymel in control of mild to moderate fatty liver

Not Applicable
Recruiting
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
Inclusion Criteria

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

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
Bmi. Timepoint: at baseline and 2 month after intervention. Method of measurement: kg/m2.
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