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Investigating the effect of garlic and curcumin on non-alcoholic fatty liver

Investigating the effect of garlic and curcumin on non-invasive liver parameters in patients with non-alcoholic fatty liver disease

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241103063584N1
Enrollment
80
Registered
2025-01-03
Start date
2024-12-21
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. Fatty (change of) liver, not elsewhere classified

Interventions

Intervention 1: For 12 weeks, garlic and curcumin tablets manufactured by Mehr and Mah Pharmaceuticals are prescribed to 40 people (Garlinovus tablets containing garlic extract (500 mg) and vitamins B

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor
Mehr and Mah Pharmaceutical Knowledge enterprise Company
Collaborator

Eligibility

Sex/Gender
All
Age
15 Years to 75 Years

Inclusion criteria

Inclusion criteria: Having AST and ALT above 33 in men and 25 in women Having at least one of the following: a- diabetes b- hyperlipidemia c- obesity Age 15 to 75 years old No consumption or no history of alcohol consumption No positive viral hepatitis serology (B,C,...) ANA or AMA tests, a1 antitrypsin, serum level of ceruloplasmin, level of ASMA antibodies and LKM1 and coagulation tests and serum albumin are normal. Absence of ferritin above 450 or 45% <IRON / TIBC The patient does not have coagulation disorders. Before the intervention, the patient should not have an acute or chronic disease that causes LFT (liver function tests) disorders. Before the study, the patient should take medication that has the potential to disrupt LFT. Presence of fatty liver in ultrasound

Exclusion criteria

Exclusion criteria: During the intervention, the patient suffers from an acute or chronic disease that causes a disturbance in LFT (liver function tests). The patient should take medication during the study that has the potential to disrupt LFT. Get pregnant during the study. The patient's unwillingness to continue cooperation during the study

Design outcomes

Primary

MeasureTime frame
Amount of liver laboratory test. Timepoint: At the beginning of the study (before the start of the intervention) and 12 weeks after the start of taking garlic and curcumin tablets. Method of measurement: Fibro scan and laboratory tests.

Secondary

MeasureTime frame
Fibro scan changes. Timepoint: At the beginning of the study (before the start of the intervention) and 12 weeks after the start of taking garlic and curcumin tablets. Method of measurement: Fibroscan device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Beheshtinamdar

Mashhad University of Medical Sciences

BeheshtiA@mums.ac.ir+98 51 3853 6962

Outcome results

None listed

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