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A randomized, double-blind, placebo-, and positive-controlled clinical pilot study to evaluate the efficacy and tolerability of standardized aqueous extracts of Terminalia chebula and Terminalia bellerica in subjects with hyperuricemia
The exact scheme of treatment is made individually, taking into account age
Adding 2 mL creates a 15 mg/mL concentration
This provides preliminary human evidence that the tested formulation reached biologically relevant compartments
This dose was chosen based on a previous dose-escalation study and subsequent work demonstrating its efficacy to drive weight loss in a short period of time 8
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