The Metabolic Effects of Ginseng Oligopeptide Preparation on Non- Alcoholic Fatty Liver Disease With Obesity: a Randomized Controlled Double-blind Trial
Ginseng oligopeptide (Ginseng extract)
+ Maltodextrin
Digestive System Diseases+1
+ Fatty Liver
+ Liver Diseases
Treatment Study
Summary
Study start date: December 25, 2023
Actual date on which the first participant was enrolled.This study focuses on understanding how ginseng oligopeptide might help people suffering from non-alcoholic fatty liver disease who are also dealing with obesity. The main goal is to see if this natural compound can be an effective way to prevent and treat this liver condition. Non-alcoholic fatty liver disease is a common issue, especially among those with obesity, and finding new, effective ways to manage it is important for improving the health and quality of life for many people. Participants in this study are divided into two groups. One group receives the ginseng oligopeptide by mouth, while the other group receives a placebo, which is a harmless pill with no active ingredients. Researchers are measuring several health indicators, such as liver function, blood lipid levels, and blood glucose, as well as conducting liver ultrasounds to observe any changes. This helps determine how effective the ginseng oligopeptide is at improving liver health and managing the disease. The study aims to provide insights into how this treatment might benefit individuals with this condition.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.200 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives