Enhancing effect of supplement on resting energy metabolism after single oral intake. -A randomized, double blind, placebo controlled, cross-over study
- Conditions
- Adult males
- Registration Number
- JPRN-UMIN000035586
- Lead Sponsor
- FANCL Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 20
Not provided
1)Subjects who are undergoing medication suffer from some sort of disease. 2)Subjects who being irregular daily life such as shift worker or midnight work. 3)Subjects who have allergy to the test food or the provided meals and have potentially cause severe allergies to other foods and medicine. 4)Subjects who are likely to develop allergic rhinitis including pollinosis of moderate or higher symptoms during the study period. 5)Subjects who are plans to use medicines, quasi-drugs, food with health claims (food for specified health use), health foods and dietary supplements during the study period. 6)Subjects who have serious medical history or current medical history for liver, kidney, pancreas, heart, lung, circulatory organ, digestive organ, blood, metabolism. 7)Subjects whose HbA1c(NGSP) is more than 6.5 % 8)Subjects who have a habit of smoking. 9)Subjects who are ingesting alcohol in excessive (alcohol in terms of 60 g or more per day). 10)Subjects whose blood donation is more than 200 mL in the past one month or more than 400 mL in the past three months. 11)Subjects who have participated in other clinical trial or whose three months have not elapsed after joining other clinical trials or who have plans to participate in other clinical trials after consented to participation in this study. 12)Subjects who is considered to be inappropriate to attend the present study by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method