Probiotic
Dietary SupplementProbiotic-Lactobacillus Zeae and Lactobacillus reuteri
NCT Number: NCT06491342
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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Notify Me20 year–80 year
All sexes
Interventional
Not applicable
Division of gastroenterology and hepatology, Ratchathewi, Bangkok, Thailand
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
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
Probiotic-Lactobacillus Zeae and Lactobacillus reuteri
placebo
Time frame: 12 weeks
Shear wave velocity with controlled attenuation parameter (CAP) unit in decibels per meter (dB/m)
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
Time frame: 12 weeks
Fibroscan- transient elastography in kilopascals (kPa)
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)
Time frame: 12 weeks
Fasting plasma glucose (FPG) in mg/dL
Time frame: 12 weeks
HbA1C in percent
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
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
Time frame: 12 weeks
hsCRP level in mg/L
Time frame: 12 weeks
Interleukin 6 (IL-6) in pg/mL
Time frame: 12 weeks
Weight and height will be combined to report BMI in kg/m^2
Time frame: 12 weeks
Body fat in percentage
Time frame: 12 weeks
Body muscle in kilogram
Time frame: 12 weeks
Fecal SCFA (acetate, propionate and butyrate) in microgram/ml metagenomic sequencing (Next-generation sequencing)
Phramongkutklao College of Medicine and Hospital
Other
PROBIOTIC SUPPLEMENT VERSUS PLACEBO FOR DECREASE STEATOSIS IN METABOLIC DYSFUNCTION-ASSOCIATED STEATOTIC LIVER DISEASE (MASLD): A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL
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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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