Geneva, Aug. 29 -- International Clinical Trials Registry received information related to the study (JPRN-UMIN000058797) titled 'Effects of lactic acid bacteria ingestion on subjective physical symptoms in healthy adult: A randomized, double-blind, placebo-controlled, parallel group comparison study' on Aug. 13.
Study Type: Interventional
Study Design:
Parallel Randomized
Primary Sponsor: KSO corporation
Condition:
Healthy adults
Intervention:
Daily ingestion of powdered lactic acid bacteria for 12 weeks.
Daily ingestion of placebo powder for 12 weeks....
Recruitment Status: Not Recruiting
Phase: Not applicable
Date of First Enrollment: 2025/10/11
Target Sample Size: 200
Countries of Recruitment:
Japan
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