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Efficacy of Silymarin and Vitamin E in the Treatment fatty liver

The Efficacy of Silymarin and Vitamin E in the Treatment of the Non-Alcoholic Fatty Liver Disease: A Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20081110001444N6
Enrollment
80
Registered
2019-11-02
Start date
2014-04-01
Completion date
Unknown
Last updated
2019-11-05

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. Nonalcoholic steatohepatitis (NASH)

Interventions

Intervention 1: Intervention group 1 silymarin: Silymarin 140 mg BID (with the brand name of Livergol from Goldaru Pharmaceutical Company, Iran) for four months.Additionally, they were all given consu

Sponsors

Shahid Sadoughi University of Medical Sciences-Yazd, Iran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria were : NAFLD confirmed through abdominal ultrasonography, persistent elevation in the level of alanine aminotransferase (ALT) within the last six months for one and a half times more than the upper normal limit, fatty changes diagnosed through ultrasonography, and over 20 years of age.

Exclusion criteria

Exclusion criteria: The exclusion criteria were autoimmune hepatitis, alpha-1 antitrypsin deficiency, chronic hepatitis B or C, hemochromatosis, and Wilson’s disease. Patients with a history of diabetes, daily consumption ethanol, severe cardiac, pulmonary, renal, or psychological problems, positive pregnancy test, and the use of drugs such as statins, fibrates, anti-convulsants, NSAID, acetaminophen, warfarin, metronidazole, anti-depressants, or anti-psychotics were also excluded from the study.

Design outcomes

Primary

MeasureTime frame
ALanin aminotransferas measurements. Timepoint: They were received at the baseline and then after four months for ALT measurements. Method of measurement: autoanlizer.;Ultrasonographic evaluations of their liver. Timepoint: first and four months later. Method of measurement: General Electric ultrasound device,.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmohsen akhondi-Meybodi

Yazd University of Medical Sciences

akhondei@yahoo.com+98 35 3827 4543

Outcome results

None listed

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