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An 8-wk, randomized, double-blind, placebo-controlled clinical trial for the antidiabetic effects of hydrolyzed ginseng extract.


ABSTRACT: BACKGROUND:To investigate the antidiabetic effects of hydrolyzed ginseng extract (HGE) for Korean participants in an 8-wk, randomized, double-blinded, placebo-controlled clinical trial. METHODS:Impaired fasting glucose participants [fasting plasma glucose (FPG) ? 5.6mM or < 6.9mM] who had not been diagnosed with any disease and met the inclusion criteria were recruited for this study. The 23 participants were randomly divided into either the HGE (n = 12, 960 mg/d) or placebo (n = 11) group. Outcomes included measurements of efficacy (FPG, postprandial glucose, fasting plasma insulin, postprandial insulin, homeostatic model assessment-insulin resistance, and homeostatic model assessment-?) and safety (adverse events, laboratory tests, electrocardiogram, and vital signs). RESULTS:After 8 wk of HGE supplementation, FPG and postprandial glucose were significantly decreased in the HGE group compared to the placebo group. No clinically significant changes in any safety parameter were observed. Our study revealed that HGE is a potent antidiabetic agent that does not produce noticeable adverse effects. CONCLUSION:HGE supplementation may be effective for treating impaired fasting glucose individuals.

SUBMITTER: Park SH 

PROVIDER: S-EPMC4213818 | biostudies-literature | 2014 Oct

REPOSITORIES: biostudies-literature

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An 8-wk, randomized, double-blind, placebo-controlled clinical trial for the antidiabetic effects of hydrolyzed ginseng extract.

Park Soo-Hyun SH   Oh Mi-Ra MR   Choi Eun-Kyung EK   Kim Min-Gul MG   Ha Ki-Chan KC   Lee Seung-Kwon SK   Kim Young-Gon YG   Park Byung-Hyun BH   Kim Dal-Sik DS   Chae Soo-Wan SW  

Journal of ginseng research 20140523 4


<h4>Background</h4>To investigate the antidiabetic effects of hydrolyzed ginseng extract (HGE) for Korean participants in an 8-wk, randomized, double-blinded, placebo-controlled clinical trial.<h4>Methods</h4>Impaired fasting glucose participants [fasting plasma glucose (FPG) ≥ 5.6mM or < 6.9mM] who had not been diagnosed with any disease and met the inclusion criteria were recruited for this study. The 23 participants were randomly divided into either the HGE (n = 12, 960 mg/d) or placebo (n =   ...[more]

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