Tokyo, June 29 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058303) titled 'A Pre- and Post- Comparative Study on the Intestinal Delivery of Probiotics in Neonates with Two Different Dosages' on June 29.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Randomized
Blinding - Single blind -participants are blinded
Control - Dose comparison
Primary Sponsor:
Institute - KSO Corporation
Condition:
Condition - None
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To exploratively evaluate the intestinal delivery of probiotics, changes in the gut environment, and effects on health when healthy neonates consume tes...