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Clinical Trials/JPRN-UMIN000049183
JPRN-UMIN000049183
Completed
未知

A clinical study for evaluating the effects of food containing lactic acid bacteria on common cold symptoms - A randomized, double-blind, placebo-controlled, parallel-group comparative method - - A clinical study for evaluating the effects of food containing lactic acid bacteria on common cold symptoms

KSO Corporation0 sites200 target enrollmentOctober 12, 2022
ConditionsHealthy Adults

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy Adults
Sponsor
KSO Corporation
Enrollment
200
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 12, 2022
End Date
April 16, 2023
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Participants (who) 1\. suffering from, undergoing treatment for, or with a history of serious diseases 2\. have chronic diseases and take medication on a daily basis 3\. have been diagnosed with dry mouth 4\. are unable to abstain from taking supplement, food for specified health use or functional food, or health food that may affect immune function 5\. are unable to abstain from taking food that containing lactic acid bacteria, bifidobacterium, oligosaccharides, or viable bacteria during the study 6\. consistently drink more than the appropriate amount of alcohol 7\. are unable to abstain from alcohol for 2 days prior to the screening test and each test 8\. have food allergies 9\. take or plan to take medicine for pollen allergy 10\. with digestive diseases affecting digestion and absorption and those with a history of digestive surgery (excluding appendicitis) 11\. tend to get diarrhea by taking dairy products 12\. are pregnant women, women who intend to become pregnant during the research period, and women who are breastfeeding 13\. are judged to be inappropriate as research participants based on blood tests in the screening tests 14\. have a history or current condition of drug or alcohol dependence 15\. are participating in research involving the ingestion of other foods or the use of other medicines or those who have participated in or are willing to participate in other clinical research within one month of obtaining consent 16\. are judged to be inappropriate as research participants by the principal investigator 17\. smoke 21 or more cigarettes a day 18\. plan to receive the influenza vaccine from 3 weeks before ingestion to the end of the ingestion period 19\. plan to receive the COVID\-19 vaccine during the ingestion period 20\. work on night shift 21\. plan to travel abroad during the study 22\. has donated more than 200 mL of blood within 1 month or 400 mL of blood within 3 months prior to the date of obtaining consent, or those who have donated blood components

Outcomes

Primary Outcomes

Not specified

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