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A study for evaluating the effect of the intake of a Lactobacillus containing food on retaining moisture of the skin in adult female with a tendency for constipation:double blind, placebo-controlled study

Not Applicable
Conditions
tendency toward constipation
Registration Number
JPRN-UMIN000018976
Lead Sponsor
TTC Co., Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects who routinely takes foods or medicines containing of lactobacillus (2) Subjects who routinely takes foods or medicines which may influence bowel movement or skin (3) Subjects having diseases affecting bowel movement or a history of these diseases (4) Subjects who hase treated cosmetic care (5) Subjects who has treated cosmetic care except for measuring sites, or hormonal therapy for one year (6) Subjects who got a facial, a wash-rag, lost hair on measuring sites for one month ago, or plans these actions. (7) Subjects who washes the body using a nylon towel which provides strong skin irritation (8) Subjects who has the wound or inflammatory disease affecting the measuring skin (9) Subjects who has asthma or the possibility of asthma (10) Subjects who has being excepted to be developed the allergy symptoms on skin (11) Subjects who feels to trouble by rough skin around a menstruates (12) Subjects who is employed on a pre-dawn shift or on night duty more than 2 times (13) Subjects who is planned to go overseas (14) Subjects who has treatment or a history of serious disease or affecting a secretion of sex hormones (15) Subjects having possibilities for emerging allergy related to the study (16) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on screening test (17) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study (18) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating (19) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (20) Subjects judged as unsuitable for the study by the investigator for other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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