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Effect of Sim Liver Herbal Drug on the Treatment of Fatty Liver

Evaluation of the Effect of Sim Liver Herbal Drug on the Treatment of Fatty Liver

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201109049323N1
Enrollment
60
Registered
2021-01-03
Start date
2020-03-20
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Non-alcoholic fatty liver. Nonalcoholic steatohepatitis (NASH)

Interventions

Intervention 1: Intervention group: They will receive 240 mg tablets of Live Liver (Simorgh Pharmaceutical Company of Attar Drug and the country of manufacture of Iran) every 12 hours before meals wit

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of non-alcoholic fatty liver on ultrasound Diagnosis of non-alcoholic fatty liver by liver enzymes

Exclusion criteria

Exclusion criteria: Use of statins History of viral liver disease or chronic liver disease except fatty liver History of hepatitis (autoimmune and viral) Opioid users Dissatisfaction with participating in the study Patients with liver and bile duct cancers

Design outcomes

Primary

MeasureTime frame
Alanine aminotransferase. Timepoint: The beginning of the intervention, two months after the intervention. Method of measurement: Biochemistry Laboratory.;Aspartate aminotransferase. Timepoint: The beginning of the intervention, two months after the intervention. Method of measurement: Biochemistry Laboratory.;Weight. Timepoint: The beginning of the intervention, two months after the intervention. Method of measurement: Digital balance.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamira Kafshi

Islamic Azad University

samira.kfh@gmail.com+98 41 3432 3456

Outcome results

None listed

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