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The effect of camelina oil in patients with nonalcoholic fatty liver

Comparison of the effects of Camelina and Sunflower oils on metabolic, inflammatory and anti-inflammatory factors in patients with Non-alcoholic fatty liver

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150205020965N5
Enrollment
46
Registered
2019-12-13
Start date
2019-11-20
Completion date
Unknown
Last updated
2020-08-17

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: In this study, Camelina oil will be replaced with 15% of the daily total fat intake for three months. Then, 15 days before the beginning of study, FFQ questionnaire will be completed f

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age range 20 to 65 years BMI=25 No weight changes over the past 3 months Restricted Consumption of edible nuts and fish Tendency to use camelina oil Having grade 1 and 2 of non-alcoholic fatty liver disease

Exclusion criteria

Exclusion criteria: Having other liver disease apart from NAFLD (alcoholic fatty liver, viral hepatitis, cirrhosis and biliary obstruction, liver cancer)) Liver transplantation Pregnancy and Lactation Kidney, Cardiovascular Disease Alcohol and tobacco consumption high physical activity having acute illness Use of drugs such as glucocorticoids, nonsteroidal anti-inflammatory drugs (NSAIDS), hepatotoxic drugs, antibiotics Use antioxidant supplements and W3 history of using weight loss diet or a special diet over the past 6 months

Design outcomes

Secondary

MeasureTime frame
Body Mass Index (BMI). Timepoint: At baseline and three months after baseline. Method of measurement: Scale-Meter.;Amount of received energy. Timepoint: At baseline and three months after baseline. Method of measurement: questionnaire.;Daily macronutrient intake (carbohydrate, protein, fat). Timepoint: At baseline and three months after baseline. Method of measurement: questionnaire.;Waist circumference (WHR). Timepoint: At baseline and three months after baseline. Method of measurement: Calculate by splitting waist to hip.;Blood pressure. Timepoint: At baseline and three months after baseline. Method of measurement: Mercuric barometr.;Assessment of the body composition. Timepoint: At baseline and three months after baseline. Method of measurement: BIA devices.

Primary

MeasureTime frame
ALT. Timepoint: At baseline and three months after baseline. Method of measurement: Hitachi 911 auto-analyzer.;AST. Timepoint: At baseline and three months after baseline. Method of measurement: Hitachi 911 auto-analyzer.;ALP. Timepoint: At baseline and three months after baseline. Method of measurement: Hitachi 911 auto-analyzer.;Degree of hepatic steatosis. Timepoint: At baseline and three months after baseline. Method of measurement: Ultrasound.;Fasting glucose. Timepoint: At baseline and three months after baseline. Method of measurement: Hitachi 911 auto-analyzer.;Insulin Sensitivity Index (QUICK). Timepoint: At baseline and three months after baseline. Method of measurement: Computing.;Insulin Resistance Index (HOMA-IR). Timepoint: At baseline and three months after baseline. Method of measurement: Computing.;Fasting insulin. Timepoint: At baseline and three months after baseline. Method of measurement: Chemoluminescense.;Total cholestrol. Timepoint: At baseline and three months after baseline. Method of measurement: Hitachi 911 auto-analyzer.;HDL-cholesterol. Timepoint: At baseline and three months after baseline. Method of measurement: Hitachi 911 auto-analyzer.;LDL-cholesterol. Timepoint: At baseline and three months after baseline. Method of measurement: calculation of LDL using friedewald equation.;Triglyceride. Timepoint: At baseline and three months after baseline. Method of measurement: Hitachi 911 auto-analyzer.;Highly sensitive C-reactive protein(hs-CRP ). Timepoint: At baseline and three months after baseline. Method of measurement: ELISA Dedicated Kit.;Tumor Necrosis Factor(TNF). Timepoint: At baseline and three months after baseline. Method of measurement: ELISA Dedicated Kit.;Interleukin 10(IL10 ). Timepoint: At baseline and three months after baseline. Method of measurement: ELISA Dedicated Kit.;Total antioxidant capacity. Timepoint: At baseline and three months after baseline. Method of measurement: kit.;Malondialdehyde. Timepoint: At baseline

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParvin Dehghan

Tabriz University of Medical Sciences

dehghan.nut@gmail.com+98 33340634

Outcome results

None listed

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