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A probiotic powder intervention developed and studied by The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School. It is currently being evaluated in a randomized, double-blind clinical trial (NCT03756623) to assess its impact on gut microbiome composition and metabolic markers in healthy individuals. The intervention consists of 0.5g of probiotic powder administered orally three times daily over a 12-week period. The study aims to characterize changes in gut microbiota and their correlation with metabolic parameters such as fasting glucose, insulin levels, and lipid profiles, comparing the effects to those of metformin and a placebo.
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