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A Clinical Study to Evaluate the Effect of SIM01 in Female With NAFLD - Trial NCT05885373

Access comprehensive clinical trial information for NCT05885373 through Pure Global AI's free database. This phase not specified trial is sponsored by GenieBiome Limited and is currently Recruiting. The study focuses on Non-Alcoholic Fatty Liver Disease. Target enrollment is 40 participants.

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NCT05885373
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dietary supplement
Trial Details
ClinicalTrials.gov โ€ข NCT05885373
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A Clinical Study to Evaluate the Effect of SIM01 in Female With NAFLD
A Single-arm, Open-label Clinical Study to Evaluate the Effect of SIM01 in Female Subjects With Non-Alcoholic Fatty Liver Disease (NAFLD)

Study Focus

SIM01

Interventional

dietary supplement

Sponsor & Location

GenieBiome Limited

Hong Kong, China

Timeline & Enrollment

N/A

Mar 01, 2023

Dec 31, 2023

40 participants

Primary Outcome

Change in CAP score by fibroscan after taking SIM01 for 3 months

Summary

Non-alcoholic fatty liver disease is one of the most common chronic liver diseases worldwide.
 Available data indicates that probiotics may regulate the gut microbiota and improve liver
 function in females with non-alcoholic fatty liver disease. In this study, we aim to
 investigate if the synbiotics (prebiotics and probiotics) are efficacious subjects in liver
 function improvement in female subjects with Non-alcoholic fatty liver disease.

ICD-10 Classifications

Alcoholic fatty liver
Alcoholic liver disease, unspecified
Alcoholic liver disease
Liver disease, unspecified
Alcoholic cirrhosis of liver

Data Source

ClinicalTrials.gov

NCT05885373

Non-Device Trial