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Completed

NCT Number: NCT06491342

Probiotic Supplement Versus Placebo for the Treatment of Patients With Non-alcoholic Fatty Liver Disease

Probiotic supplement versus placebo for the treatment of patients with non-alcoholic fatty liver disease: a randomized, double-blind, placebo-controlled trial

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Division of gastroenterology and hepatology, Ratchathewi, Bangkok, Thailand

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About this study

Probiotic supplement versus placebo for the treatment of patients with non-alcoholic fatty liver disease: a randomized, double-blind, placebo-controlled trial by access liver biochemistry, MRI-PDFF, fibroscan and metabolic profile

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Male and female adults ≥20,<80 years of age who suspected or confirmed diagnosis of NASH/NAFLD suggested by the historical data, they must meet one of the following criteria:

Fatty liver by imaging then fibroScan with CAP ≥ 248 dB m Liver biopsy compatible with NASH/NAFLD

Exclusion criteria

  • Supplement with probiotic/prebiotic within 2 weeks
  • Previous antibiotic/antifungus within 1 month
  • History of significant alcohol consumption for a period of more than three consecutive months within 1 year before screening. Significant alcohol consumption is defined as equal to or greater than approximately two alcoholic drinks per day for males and approximately 1.5 alcoholic drinks per day for females
  • Regular use of drugs historically associated with NAFLD, which include, but are not limited, to the following: amiodarone, methotrexate, systemic glucocorticoids at greater than 5 mg/d
  • Chronic liver diseases from other cause such as viral hepatitis, autoimmune hepatitis
  • Hepatic decompensation or impairment defined as presence of any of the following:
  • History of esophageal varices, ascites or hepatic encephalopathy.
  • Serum albumin <3.5 g dl-1, except as explained by nonhepatic causes.
  • INR > 1.4
  • Use of GLP-1 agonist therapy (for example, exenatide, liraglutide, lixisenatide, albiglutide, dulaglutide, semaglutide and albiglutide), vitamin E and pioglitazone
  • Active autoimmune disease, including actively treated lupus, rheumatoid arthritis, inflammatory bowel disease
  • Active malignancy on treatment
  • New York Heart Association Class III or IV heart failure or known left ventricular ejection fraction <30%
  • Known immunocompromised status, HIV or who have recurrent or chronic systemic bacterial, fungal, viral or protozoal infections
  • Respiratory compromised
  • Severe renal impairment (eGFR <30 ml/min/1.73 m2)
  • Pregnancy

Treatment and study plan

Probiotic

Dietary Supplement

Probiotic-Lactobacillus Zeae and Lactobacillus reuteri

Placebo

Dietary Supplement

placebo

Primary outcomes

  1. Liver steatosis by fibroscan

    Time frame: 12 weeks

    Shear wave velocity with controlled attenuation parameter (CAP) unit in decibels per meter (dB/m)

  2. Liver steatosis by MRI

    Time frame: 12 weeks

    Hepatic steatosis with MRI-PDFF (the percent ratio of the density of mobile protons from triglycerides and the total density of protons from mobile triglycerides and mobile water). Outcome Measures was report as percent

  3. Liver stiffness by fibroscan

    Time frame: 12 weeks

    Fibroscan- transient elastography in kilopascals (kPa)

Secondary outcomes

  1. Liver inflammation

    Time frame: 12 weeks

    Evaluated alanine aminotransferase (ALT; U/L), aspartate aminotransferase (AST; U/L), gamma-glutamyl transferase (GGT; U/L), and alkaline phosphatase (ALP; U/L)

  2. Metabolic profile

    Time frame: 12 weeks

    Fasting plasma glucose (FPG) in mg/dL

  3. Metabolic profile

    Time frame: 12 weeks

    HbA1C in percent

  4. Metabolic profile: HOMA IR

    Time frame: 12 weeks

    Fasting plasma glucose and serum insulin level will be combined to report in HOMA IR in mg/dl x mIU/L

  5. Metabolic profile: serum lipid profiles

    Time frame: 12 weeks

    Total cholesterol in mg/dL, low-density lipoprotein (LDL) cholesterol in mg/dL, high-density lipoprotein (HDL) in mg/dl, cholesterol in mg/dL, and triglyceride in mg/dL

  6. Inflammatory marker

    Time frame: 12 weeks

    hsCRP level in mg/L

  7. Inflammatory marker

    Time frame: 12 weeks

    Interleukin 6 (IL-6) in pg/mL

  8. Anthropomorphic evaluation: BMI

    Time frame: 12 weeks

    Weight and height will be combined to report BMI in kg/m^2

  9. Anthropomorphic evaluation: composition analysis

    Time frame: 12 weeks

    Body fat in percentage

  10. Anthropomorphic evaluation

    Time frame: 12 weeks

    Body muscle in kilogram

Other outcomes

  1. Fecal SCFA

    Time frame: 12 weeks

    Fecal SCFA (acetate, propionate and butyrate) in microgram/ml metagenomic sequencing (Next-generation sequencing)

Sponsors and collaborators

Lead sponsor

Phramongkutklao College of Medicine and Hospital

Other

Collaborators

  • Chiang Mai University
  • Thailand Institute of scientific and technological research

Registry information

Official study title

PROBIOTIC SUPPLEMENT VERSUS PLACEBO FOR DECREASE STEATOSIS IN METABOLIC DYSFUNCTION-ASSOCIATED STEATOTIC LIVER DISEASE (MASLD): A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jul 9, 2024
Registry last updated
Jul 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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