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The effect of resveratrol supplementation along with interval training on liver enzymes, inflammatory factors and oxidative stress indices in patients with non-alcoholic fatty liver disease (NAFLD): a double-blind randomized clinical trial.

The effect of resveratrol supplementation along with interval training on liver enzymes, inflammatory factors and oxidative stress indices in patients with non-alcoholic fatty liver disease (NAFLD): a double-blind randomized clinical trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240604062009N1
Enrollment
48
Registered
2024-11-25
Start date
2023-06-22
Completion date
Unknown
Last updated
2025-01-08

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 (NAFLD). Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: intervention group: Patients in the groups receiving resveratrol supplement received 1 capsule of 400 mg daily, one hour after meals for 8 weeks. In order to assign the supplement, fir

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the research Men aged 45-60 years Suffering from non-alcoholic fatty liver grade 1-3 based on laboratory and ultrasound methods

Exclusion criteria

Exclusion criteria: Unwillingness to participate in the study Use of any nutritional supplement (omega-3 supplement) or supplements that have anti-inflammatory and antioxidant properties in the last 3 months or during the study. Suffering from kidney failure, cardiovascular diseases, breast cancer and thyroid diseases. Smoking and alcohol consumption Patients using NSAIDs, corticosteroids (prednisone, prednisolone and hydrocortisone), thiazide diuretics (furosemide and hydrochlorothiazide) and second generation antipsychotics (olanzapine and clozapine). have taken these drugs and during the study people were advised to refrain from taking these drugs.)

Design outcomes

Primary

MeasureTime frame
Determining the effect of resveratrol supplementation along with intermittent exercises on ALT enzyme changes in patients with non-alcoholic fatty liver disease (NAFLD) in intervention and control groups. Timepoint: Eight Weeks. Method of measurement: Before and after the intervention, venous blood samples were taken from all participants after 12-14 hours of fasting, and after serum separation by centrifugation, serum ALT was measured by ELISA method.;Determining the effect of taking resveratrol supplement along with intermittent exercises on AST enzyme changes in patients with non-alcoholic fatty liver disease (NAFLD) in intervention and control groups. Timepoint: Eight Weeks. Method of measurement: Before and after the intervention, venous blood samples were taken from all participants after 12-14 hours of fasting, and after serum separation by centrifugation, serum AST was measured by ELISA method.;Determining the effect of taking resveratrol supplement along with intermittent exercises on changes in total antioxidant capacity (TAC) in patients with non-alcoholic fatty liver disease (NAFLD) in intervention and control groups. Timepoint: Eight Weeks. Method of measurement: Plasma TAC was measured by spectrophotometric method and using RANDOX kit, by autoanalyzer (Abbot Model Aclyon 300).;Determining the effect of taking resveratrol supplement along with periodic exercises on malondialdehyde (MDA) changes in patients with non-alcoholic fatty liver disease (NAFLD) in intervention and control groups. Timepoint: Eight Weeks. Method of measurement: The basis of the serum MDA measurement method is based on the reaction with thiobarbituric acid (TBA), extraction with normal butanol, measuring the absorbance of Barosh spectrophotometry and comparing the absorbance with the standard curve.;Determining the effect of resveratrol supplementation along with intermittent exercises on the changes of interleukin-6 (IL-6) in patients with non-alcoholic fatty liver disease (NAFLD)

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZaher Etemad

Islamic Azad University

zetemad2002@yahoo.com+98 918 174 1523

Outcome results

None listed

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