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Milk thistle (Silymarin marianum) extract supplementation on nonalcoholic fatty liver disease

Effect of milk thistle (Silymarin marianum) extract supplementation on nonalcoholic fatty liver disease in morbidly-obese patient candidates for bariatric surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210817052218N1
Enrollment
50
Registered
2021-12-01
Start date
2021-12-16
Completion date
Unknown
Last updated
2022-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Morbid obesity and non alchoholic liver diseade. Overweight and obesity

Interventions

Intervention 1: Intervention group: 500 kcal.day deficit from their normal weight-maintaining caloric intake plus taking 140 mg of Silymarin in tablet form, four times daily, for a total of 560 mg for

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: patients aged between 18 and 65 years morbidly-obese patients candidates for bariatric surgery , BMI above 40 kg/m2 Diagnosis of NAFLD in liver sonography (grades II and III steatosis) with increased levels of liver enzymes aspartate transaminase (AST) and alanine transaminase (ALT) (above 20 mg/dl for women and 30 mg/dl for men)

Exclusion criteria

Exclusion criteria: history of alcohol consumption diabetes mellitus chronic liver disease use of drugs such as statin, fibrate, non-steroidal anti-inflammatory drugs (NSAIDs), positive results for tests of autoimmune hepatitis and virus markers (hepatitis B surface antigen, hepatitis C virus antibody) unwilling to participate in study

Design outcomes

Primary

MeasureTime frame
Aspartate aminotransferase/alanine aminotransferase ratio. Timepoint: before and after two months of treatment. Method of measurement: Blood sample.;BMI (body mass index). Timepoint: before and after two months of treatment. Method of measurement: scale.;Non alchoholic fatty liver disease. Timepoint: before and after two months of treatment. Method of measurement: Sonography.;Liver fibrosis. Timepoint: before and after two months of treatment. Method of measurement: Fibroscan Metavir.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Hadi Mirhashemi

Shahid Beheshti University of Medical Sciences

sh.mirhashemi@gmail.com+98 21 23871

Outcome results

None listed

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