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Treatment effects of familact Probiotic in Non Alcoholic Fatty Liver Disease(NAFLD)

Treatment effects of familact Probiotic in Non Alcoholic Fatty Liver Disease(NAFLD)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014112019554N2
Enrollment
90
Registered
2015-07-12
Start date
2015-06-22
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

Nonalcoholic steatohepatitis. Other specified inflammatory liver diseases, Nonalcoholic steatohepatitis [NASH]

Interventions

Intervention 1: Daily exercise for at least 30 minutes. Intervention 2: Familact capsule 500 mg once daily after a meal.
Lifestyle
Treatment - Drugs
Daily exercise for at least 30 minutes
Familact capsule 500 mg once daily after a meal

Sponsors

Zanjan University of Medical Sciences, Deputy of Research and Technology, Research Management
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with NAFLD on ultrasonography; ALT more than 1.5 to 5 times the normal range; BMI between 25 to 29.9 Exclusion criteria: alcoholic hepatitis; systemic or metabolic or inflammatory disease such as diabetes; viral hepatitis; autoimmune hepatitis; secondary fatty liver disease such as drug induced fatty liver disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood pressure. Timepoint: at the first and after 8 weeks. Method of measurement: Manometer.;Body mass index. Timepoint: at the first and after 8 weeks. Method of measurement: Analog scale, Meter.;Fasting blood glucose. Timepoint: at the first and after 8 weeks. Method of measurement: ELISA.;Total cholestrol. Timepoint: at the first and after 8 weeks. Method of measurement: ELISA.;LDL. Timepoint: at the first and after 8 weeks. Method of measurement: ELISA.;HDL?. Timepoint: at the first and after 8 weeks. Method of measurement: ELISA.;TG. Timepoint: at the first and after 8 weeks. Method of measurement: ELISA.;AST. Timepoint: at the first and after 8 weeks. Method of measurement: ELISA.;ALT. Timepoint: at the first and after 8 weeks. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Maryam Jameshorani

Zanjan University of Medical Sciences

dr.shirinjameshorani@yahoo.com00

Outcome results

None listed

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