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The Metabolic Effects of Ginseng Oligopeptide Preparation on Non- Alcoholic Fatty Liver Disease With Obesity: a Randomized Controlled Double-blind Trial

Not Applicable
Not yet recruiting
Conditions
Non-alcoholic Fatty Liver Disease
Interventions
Other: Maltodextrin
Other: Ginseng oligopeptide (Ginseng extract)
Registration Number
NCT06167902
Lead Sponsor
Peking Union Medical College Hospital
Brief Summary

To investigate the effect of ginseng oligopeptide on nonalcoholic fatty liver disease with obesity and clarify its intervention mechanism in theory, which will contribute to the prevention and treatment of non-alcoholic fatty liver more scientifically and effectively.The patients were randomly divided into two groups. One group of patients took ginseng oligopeptide orally, and the other group took placebo. The liver function, blood lipid, blood glucose, liver B ultrasound and other indicators were observed to further determine the efficacy.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Meet the diagnostic criteria for non-alcoholic fatty liver disease ;
  • Aged 18-65 years old;
  • ALT, AST, GGT≤2×Upper Limit Of Normal(ULN);
  • BMI≥28Kg/㎡;
  • Patients signed the relevant informed consent on a voluntary basis.
Exclusion Criteria
  • Under 18 years old and over 65 years old;
  • Allergic to the ingredients of ginseng oligopeptide preparation;
  • Serum ALT, AST, GGT>2ULN;
  • Currently taking oral hepatoprotective drugs such as reduced glutathione, polyene phosphatidylcholine, and silibinin, etc.;
  • Subjects participating in other clinical trials;
  • Pregnant or lactating women;
  • Complicated with serious diseases of the digestive system or other systems, such as chronic gastrointestinal diseases and chronic diseases causing digestive malabsorption,Kidney disease, hematological system or autoimmune diseases;
  • Other populations that were deemed by the investigators to be ineligible for the trial may reduce or complicate enrollment patients with chemotherapy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
The placebo groupMaltodextrin-
Ginseng oligopeptide groupGinseng oligopeptide (Ginseng extract)-
Primary Outcome Measures
NameTimeMethod
aspartate aminotransferase (AST)The day of enrollment, day 60 and day 120 after enrollment.

Liver function

Alanine aminotransferase (ALT)The day of enrollment, day 60 and day 120 after enrollment.

Liver function

glutamyltransferase (GGT).The day of enrollment, day 60 and day 120 after enrollment.

Liver function

Secondary Outcome Measures
NameTimeMethod
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