Study of the effect of a drink containing lactic acid bacteria on feeling of tiredness.
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000041272
- Lead Sponsor
- APO PLUS STATION CO., LTD.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Not provided
(1)Subjects who take medicines, quasi-drugs, supplements, health foods, etc. (2)Subjects who cannot restrict the use of medicine or health foods that may influence their bowel movements after informed consent (3)Subjects who are under treatment or have a history of serious diseases (4)Subjects visiting the hospital for diseases related to bowel movements and using drugs, or regularly using commercially available constipation medicine (5)Subjects currently undergoing treatment or with digestive diseases that affect the study or have a surgical history of digestive system (except appendicectomy) (6)Subjects with diseases affecting bowel movement or have a history of these diseases (7)Subjects who drink alcohol over 1500 mL in terms of beer or smoke over average 20 cigarettes per day (8)Subjects who have a lifestyle that affect the result of this clinical trial or who plan to have such lifestyles during the test period (9)Subjects whose feeling of tiredness is caused by pain or suspected to be induced by pain (10)Subjects who are diagnosed with chronic fatigue syndrome or insomnia (11)Subjects who are diagnosed with sleep apnea syndrome or are suspected to have it (12)Subjects with a large fluctuation on defecation during menstruation or at poor physical condition (13)Subjects who have allergies to a specific drug or food (14)Subjects who have a feeling of tiredness caused by allergies to pollen, house dust, etc (15)Subjects who have participated in other clinical trial in the past one month, who have a plan to participate in other clinical trial during the test period (16)Subjects who are planned to become pregnant after submission of informed consent for this clinical trial or are pregnant or lactating (17)Subjects who are judged as unsuitable for this clinical trial by the investigator for other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Antioxidative activity (d-ROMs, BAP, 8-OHdG), oxidative stress level defined as BAP/d-ROMs
- Secondary Outcome Measures
Name Time Method VAS questionnaire regarding feeling of tiredness, intestinal flora (amplicon sequence analysis)