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Effect of Nutri Liver Support in non alchoholic fatty liver patients.

Effect of Nutri Liver Support on liver enzyme level and lipid profile of non alcoholic fatty liver patiants.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015031721502N1
Enrollment
80
Registered
2015-06-04
Start date
2015-05-31
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Non Alcoholic Fatty liver Disease. Other specified inflammatory liver diseases Nonalcoholic steatohepatitis (NASH)

Interventions

Intervention 1: Nutri Liver Support 150 mg, oral, twice a dey for 2 months. Intervention 2: placebo, oral, twice a day for 2 months.
Treatment - Drugs
Placebo
Nutri Liver Support 150 mg, oral, twice a dey for 2 months
placebo, oral, twice a day for 2 months

Sponsors

Semnan University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 20 to 40 years old; patients who has white skin; patients who referred to the clinic for checkup; fatty liver is reported in sonography; agreement to be a part of the study; ALT level above 40. Exclusion criteria: patients that want to withdraw the study at any time; cirrhosis is reported in sonography; patients who are detected as Wilson, autoimmune hepatitis, viral hepatitis, alcoholic hepatitis, hemochromatosis; patients who are suffering from chronic liver disease; drug causes is to be considered for fatty liver; sensitive to drug; those who are affecting by drug side effects.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Alanine Aminotransferase. Timepoint: before and after intervention. Method of measurement: serum.;Aspartate Aminotransferase. Timepoint: before and after intervention. Method of measurement: serum.

Secondary

MeasureTime frame
Level of serum cholesterol. Timepoint: before and after intervention. Method of measurement: serum.;Level of serum Triglyceride. Timepoint: Before & after intervention. Method of measurement: Serum.;Low-density Lipoprotein. Timepoint: Before & after intervention. Method of measurement: Serum.;High-density Lipoprotein. Timepoint: Before & after intervention. Method of measurement: Serum.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Reza Dabiri

Semnan University of Medical Sciences

Dabirirzf@yahoo.com somayehch49@yahoo.com+98 23 3343 7844

Outcome results

None listed

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