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The effect of astaxanthin supplementation on cytokeratin 18 levels

The effect of astaxanthin supplementation on cytokeratin 18 levels in children and adolescents with non-alcoholic fatty liver

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170628034786N3
Enrollment
58
Registered
2021-04-26
Start date
2021-07-21
Completion date
Unknown
Last updated
2021-05-26

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: Control group: The placebo will be taken once a day with lunch, which is quite similar in color and size to the main medicine. Intervention 2: Intervention group: Patients in the astax

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 18 Years

Inclusion criteria

Inclusion criteria: Children with non- alcoholic fatty liver disease Age between 8-18 years old Elevation of liver enzyme more than 40 Unit/Litre Evidence of fatty liver in sonography

Exclusion criteria

Exclusion criteria: Diagnosis of liver disease other than NAFLD such as : Viral hepatitis,Autoimmune hepatitis, Diabetes, Hemochromatosis, Cirrhosis, Infectious disease, Hypothyroidism Consumption of drugs that effect on liver enzyme during last two months Alcohol consumption Discontinuing the study by the patient or his/her family

Design outcomes

Primary

MeasureTime frame
Serum level of Alanine aminotransferase. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Quantitative measurement of liver transaminase.;Serum level of Aspartate aminotransferase. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Quantitative measurement of liver transaminase.;Serum levels of cytokeratin 18. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Eliza method.

Secondary

MeasureTime frame
Body fat mass. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Inbody 270 body composition measuring device.;Lean body mass. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Inbody 270 body composition measuring device.;Body mass index. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Measurement of height and weight and ratio of weight to square of height.;Waist circumference. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Measurement with meters.;Hip circumference. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Measurement with meters.;Weight. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Measurement with scales.;Height. Timepoint: Eight weeks after treatment initiation with placebo and astaxanthin. Method of measurement: Measurement with meters.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Khademian

Esfahan University of Medical Sciences

khademian51@yahoo.com+98 31 3386 8247

Outcome results

None listed

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