A double-blind, randomized, placebo-controlled clinical study to investigate the effect of the beverage containing plant extracts
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000023491
- Lead Sponsor
- Fukuhara Clinic
- Brief Summary
There was a significant difference in primary outcome
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 150
Not provided
1.Subjects who have marked impairment of liver, kidney, heart, lung, endocrine, metabolism, nerve, or consciousness, or have DM 2.Subjects who have historical disease of circulatory system disease 3.Subjects who use drugs of glycometabolism, lipidmetabolism, or reducing high blood pressure 4.Subjects who regularly use drugs, health foods, supplements which are suggested causal relationship from the study except who agree to quit taking them 5.Subjects who have allergy related to the test foods 6.Subjects who feel bad mood by blood collection in past 7.Subjects who donated 200 mL or more of blood within a month prior to the study. 8.Subjects who participate in other clinical trials within the last 4 weeks prior to the current study 9.Heavy dinkers or heavy smokers 10.Subjects whose eating habits are extremely irregular 11.Pregnant and lactating female, or who wish to get pregnant during the study period. 12.Subjects who can not agree with preliminary explanation. 13.Subjects who are ineligible due to physician's judgment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method