Skip to content

The effect of quercetin supplementation on nonalcoholic fatty liver disease

The effect of quercetin supplementation on liver enzymes, inflammation indices, lipid profile and body composition, acompaind by colori control in nonalcoholic fatty liver disease: A randomized, double-blind, pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016060628299N1
Enrollment
110
Registered
2016-07-13
Start date
2016-07-10
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

Non Alcoholic Fatty Liver Disease. Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: Sigma quercetin supplements, 500 mg per day for 55 people in the intervention group for three months?Be taken on an empty stomach. Intervention 2: placebo supplement containing starch
Treatment - Drugs
Sigma quercetin supplements, 500 mg per day for 55 people in the intervention group for three months?Be taken on an empty stomach
placebo supplement containing starch but looks completely like the original supplementation for placebo group received 500 mg per day for 55 people for three months,Be taken on an empty stomach

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria include: a willingness to participation; age 18-65 years; non-alcoholic fatty liver diagnosed by ultrasonography and liver function test Tests( Alanine transaminase and Aspartate transaminase (more than 30u/l in men and more than 20u/l in women)) ; Lack of alcohol abuse (taking more than 10 grams per day for women and more than 30 grams per day for men); Body mass index equal to or greater than 40Kg/M2; Lack of other acute and chronic liver disorders (hepatitis B and C, etc.); Wilson's disease; cirrhosis; no history of biliary tract disease; acute heart failure disease; renal; pulmonary; infectious diseases; diabetes; cancer; inherited disorders affecting liver condition (iron storage disease, etc.); the absence of pregnancy and lactation; disease related to thyroid disorders; No history of weight loss surgery in the past year; the absence of lose weight in the past three months and In general, lack of increase or decrease in weight regimes during the three months prior to sampling; Autoimmune diseases such as primary biliary cirrhosis, autoimmune hepatitis, sclerosing cholangitis; Non-use of antioxidant supplements during one month prior to sampling; Lack of use of effective drugs against weight during the three months prior to sampling; Do not use multivitamin-minerals and drugs that are most likely associated with this disease(Antiepileptic drugs, amiodarone, corticosteroids, phenytoin, lithium, roacutan, tamoxifen, methotrexate, aspirin, 5-fluorouracil, zidovudine, a synthetic estrogen, inhibitors of hydroxymethyl glutaryl coa reductase and etc);Lack of exposure to pesticides and insecticides such as: carbon tetrachloride; trichloroethylene; Avoiding the use of drugs that are likely to overlap with quercetin; including anticoagulants, inhibitors of CYP3A4 and .... Exclusion criteria included: Not wanting to continue working; diseases that require special treatment; Reduction of more than 10% of baseline body weight during the intervention period; not consumption of more than 10% of the supplements in any follow-up period and in general, any inconsistent with the inclusion criteria

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lipid profile. Timepoint: at first and the end of study. Method of measurement: enzymathic method.;Liver enzymes. Timepoint: at first and the end of study. Method of measurement: enzymathic method.;Inflammatory markers. Timepoint: at first and the end of study. Method of measurement: ELISA method.

Secondary

MeasureTime frame
Body composition. Timepoint: at firt of the study and the end of forth,eighth and Twelfth weeks. Method of measurement: BIA.;Weight. Timepoint: at firt of the study and the end of forth,eighth and Twelfth weeks. Method of measurement: With light clothing and using Seca scales with 100 gAccuracy.;Height. Timepoint: Accuracy. Method of measurement: ???? ??? ?? ??????? ?? ?? ??? ??? ?? ??? 0.1 ????? ???.;Waist circumference. Timepoint: at firt of the study and the end of forth,eighth and Twelfth weeks. Method of measurement: Using a tape measure between the lowest gear and iliac crest with accuracy of 0.5 cm.;Hip circumference. Timepoint: at firt of the study and the end of forth,eighth and Twelfth weeks. Method of measurement: Using a tape measure at the bigest part of the hips.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahboobe Hosseinikia

Kermanshah University of Medical Sciences, School of Public Health

M.hosseinikia@yahoo.com+98 83 3422 1215

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 19, 2026