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Clinical Trial Summary

Differences in metabolites of dihydroberberine (DHB) and micellar berberine (LipoMicel®, LMB) are investigated through a randomized study involving human volunteers. Over a 24-hour period, blood samples are collected and subjected to Ultra High-Performance Liquid Chromatography-High Resolution Mass Spectrometry (UHPLC-HRMS) analysis to quantify the concentrations of berberine and its metabolites.


Clinical Trial Description

n/a


Study Design


NCT number NCT06202157
Study type Interventional
Source Factors Group of Nutritional Companies Inc.
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Status Completed
Phase N/A
Start date April 1, 2023
Completion date December 31, 2023