Tokyo, July 17 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000062185) titled 'Safety Evaluation of the High-Dose Intake of Probiotics: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Comparison Study' on July 17.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Double blind -all involved are blinded
Control - Placebo
Primary Sponsor:
Institute - TES Holdings Co., Ltd.
Condition:
Condition - None
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To evaluate the safety of consuming high dose of the test food in healthy adults.
Basic objectives2 - Safety
Intervention:
Interv...