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effect of supplementation with omega-3 in patients with non-alcoholic fatty liver (NAFL)

Investigation of mechanism of supplementation effect with omega-3 on lipid profile and peroxidation , inflammatory markers, insulin resistance and liver function in patients with non-alcoholic fatty liver (NAFL) compared with control group.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015030721358N1
Enrollment
40
Registered
2015-04-11
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

(Nonalcoholic fatty liver disease (NAFLD. (Nonalcoholic fatty liver disease (NAFLD

Interventions

Intervention 1: intervention group: Omega-3 supplement with effective dosage of 900 mg/day, 3*300 mg capsules per day for 2 month. Intervention 2: control group: 3 capsules of placebo per day for 2 mo
Treatment - Drugs
Placebo
intervention group: Omega-3 supplement with effective dosage of 900 mg/day, 3*300 mg capsules per day for 2 month
control group: 3 capsules of placebo per day for 2 month

Sponsors

Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria:patient>18 year; elevated Alanine aminotransfrase for up to 6 month before beginning of the study; lack of excessive alcohol ingestion; ultrasound examination; negative diagnostic tests for viral hepatitis; absence of other causes of liver disease. Exclusion criteria: a history of alcohol intake; the use of drugs known to be associated with liver steatosis; undernutrition; pregnantand breastfeeding women.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lipid profile. Timepoint: before intervention and 2 months after intervention. Method of measurement: mg/dl with autoanalyzer.;Inflammatory markers. Timepoint: before intervention and 2 months after intervention. Method of measurement: ELISA.;Sugar profile. Timepoint: before intervention and 2 months after intervention. Method of measurement: mg/dl with autoanalyzer.;Insulin Resistance. Timepoint: before intervention and 2 months after intervention. Method of measurement: HOMA-IR.

Secondary

MeasureTime frame
Liver enzymes. Timepoint: before intervention and 2 months after intervention. Method of measurement: Autoanalyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Saeed Shirali

Ahvaz Jundishapur University of Medical Sciences

Saeed.Shirali@gmail.com00

Outcome results

None listed

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