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The effect of Sour tea supplementation in nonalcoholic fatty liver disease.

The effect of Sour tea supplementation on liver enzymes, total antioxidant capacity, glycemic indicator, lipid profile and sonographic outcomes in patients with nonalcoholic fatty liver disease:A randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140208016529N3
Enrollment
70
Registered
2018-10-24
Start date
2018-07-23
Completion date
Unknown
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nonalcoholic Fatty Liver Disease.. Nonalcoholic steatohepatitis (NASH)

Interventions

Intervention 1: Intervention group will take 500 mg of sour tea tablets, for 8 weeks. Intervention 2: Control group will take placebo tablets with identical appearance containing starch for 8 weeks.

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
23 Years to 55 Years

Inclusion criteria

Inclusion criteria: Patients with the nonalcoholic fatty liver disease confirmed with imaging techniques. Body Mass Index (BMI) of them is greater than 24.9 and lower than 40.

Exclusion criteria

Exclusion criteria: Alcohol consumption Pregnant and lactating women Any known forms of hepatic or metabolic disease except NAFLD, such as hereditary hemochromatosis, Wilson’s disease, cirosis, other metabolic disease history of gastric bypass or intestine surgery Taking hepatotoxic drugs such as calcium channel blocker, methotrexate, amiodarone, chloroquine and anti inflammatory drugs Using antioxidant supplements Hormone Therapy Patients with a history of Cushing’s syndrome renal failure Participants with less than 80% are going to be excluded.

Design outcomes

Primary

MeasureTime frame
Liver enzymes (ALT, AST). Timepoint: The first day of the study and the last day of 8th week. Method of measurement: Using Microgram/ml - laboratory kit.;Lipid profile (TG, HDL, Total cholestrol). Timepoint: The first day of the study and the last day of 8th week. Method of measurement: laboratory kit.;Liver steatosis index. Timepoint: The first day of the study and the last day of 8th week. Method of measurement: Sonography.;Fasting blood sugar. Timepoint: The first day of the study and the last day of 8th week. Method of measurement: laboratory kit.;Total antioxidant capacity. Timepoint: The first day of the study and the last day of 8th week. Method of measurement: laboratory kit.

Secondary

MeasureTime frame
Waist to hip ratio. Timepoint: The first day of the study and the last day of 8th week. Method of measurement: Non-stretchable tape without any pressure.;Body Mass Index (BMI). Timepoint: The first day of the study and the last day of 8th week. Method of measurement: Weight (kilograms) divided by the square of height (meters).;Sistolic and diastolic blood pressure. Timepoint: The first day of the study and the last day of 8th week. Method of measurement: By mercury sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Izadi

Esfahan University of Medical Sciences

Fatemeh.Izadi1993@yahoo.com+98 31 3668 8487

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026