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The effect of phytosomal curcumin on fatty liver

Effect of phytosomal curcumin on lipid profile,fasting blood glucose, anthropometric indices, hepatic function and degree of steatosis, and liver fibrosis measured by fibroscan in non-alcoholic fatty liver patients: a double-blind clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20121216011763N39
Enrollment
60
Registered
2019-11-26
Start date
2020-04-20
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Non-alcoholic fatty liver. Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: Intervention group: phytosomal curcumin, 250 mg oral capsule, once daily for 12 weeks. Intervention 2: Control group: Placebo (maltodextrin) 250 mg orally, once daily for 12 weeks.

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor
Esfahan University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study age 18-65 years Non-alcoholic fatty liver (Grade 1-3) diagnosed by previous ultrasound

Exclusion criteria

Exclusion criteria: Pregnancy and lactation Alcoholic fatty liver disease Tobacco consumption Heart, Lung and Kidney Diseases, Hepatitis, Cirrhosis, Biliary and Immune Disorders, Diabetes, Cushing's Syndrome Intake of lipid and glucose lowering drugs, Vitamin E and D, orthoedoxic acid, phenytoin, tamoxifen, lithium, corticosteroids and methotrexate Weight loss and bariatric surgery in the last year

Design outcomes

Primary

MeasureTime frame
Aspartate amino transferase. Timepoint: Before intervention, end of intervention. Method of measurement: Enzymatic photometric.;Degree of liver fibrosis. Timepoint: Before intervention, end of intervention. Method of measurement: Fibroscan device.;Degree of liver steatosis. Timepoint: Before intervention, end of intervention. Method of measurement: Fibroscan device.;Alkaline amino transferase. Timepoint: Before intervention, end of intervention. Method of measurement: Enzymatic photometric.

Secondary

MeasureTime frame
TG. Timepoint: Before intervention, end of intervention. Method of measurement: Enzymatic.;Tch. Timepoint: Before intervention, end of intervention. Method of measurement: Enzymatic.;HDL. Timepoint: Before intervention, end of intervention. Method of measurement: Enzymatic.;LDL. Timepoint: Before intervention, end of intervention. Method of measurement: Fried Wald Equation equation.;FBS. Timepoint: Before intervention, end of intervention. Method of measurement: Enzymatic.;Weight. Timepoint: Before intervention, end of intervention. Method of measurement: Digital scale.;Waist. Timepoint: Before intervention, end of intervention. Method of measurement: Meters irreversible.;BMI. Timepoint: Before intervention, end of intervention. Method of measurement: Body Mass Index Formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholamreza Askari

Esfahan University of Medical Sciences

askari@mui.ac.ir+98 31 3668 1378

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 9, 2026