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A study for evaluating the effect of the intake of a resistant glucan (water-soluble dietary fiber)on bowel movement: randomized, double blind, placebo-controlled study

Not Applicable
Conditions
Healthy adult
Registration Number
JPRN-UMIN000019073
Lead Sponsor
TTC Co.,Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Not provided

Exclusion Criteria

(1) Subjects who routinely use food rich in dietary fiber (2) Subjects routinely taking medicine or health food which may influence bowel movement (3) Subjects having a large amount of foods which may influence bowel movement such as food containing dietary fiber , lactic acid bacteria (4) Subjects visiting the hospital for diseases related bowel movements and using drugs, or using commercial laxative (5) Subjects currently undergoing treatment with digestive diseases that affect the study or having a surgical history of digestive system (except appendicectomy) (6) Subjects having diseases (irritable enteritis, ulcerative colitis, etc.) affecting bowel movement or a history of these diseases (7) Subjects having diseases or a history of drug addiction or alcoholism (8) Subjects who has under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) (9) Subjects having possibilities for emerging allergy related to the study (10) Subjects who are under medication or having a history of serious diseases for which medication was required (11) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (12) 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 (13) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating (14) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (15) 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
defecation frequency, defecation days, stool output for 2 weeks.
Secondary Outcome Measures
NameTimeMethod
fecal condition for 2 weeks.
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