Healthy adult
Conditions
Interventions
Intake of test product,3-fold quantity for 4 weeks
Sponsors
TTC Co., Ltd
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1)Healthy males and females from 20 to 64 years of age (2)Subjects falling under any of the following answer of the lifestyle questionnaire in the preliminary examination A.Subjects with a tendency for constipation at three to five times of defecation per week B.Subjects with a tendency for constipation at seven times of defecation per week
Exclusion criteria
Exclusion criteria: (1)Subjects judged as unstable for this study based on the results of clinical examination or cardiopulmonary abnormality (2)Subjects have possibilities to develop an allergy to the test product (3)Subjects have a disease requiring regular medication or a history of serious diseases for which medication was required. (4)Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (5)Subjects who have participated in other clinical studies (6)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating (7)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (8)Subjects judged as unsuitable for the study by the investigator for other reasons
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hematologic test Biochemical test Urine analysis Blood pressure/Pulse rate Weight/body mass index Doctor's questions Adverse event Evaluate at points of 2 and 4 weeks of ingestion and 2 weeks after the end of ingestion period | — |
Countries
Japan
Contacts
Public ContactTamaki Furuhata
TTC Co., Ltd Clinical Research Planning Department
Outcome results
None listed