A study of the effect of continuous intake of test food on ketone body and lipid concentration. - an open-label trial
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000048306
- Lead Sponsor
- IMEQRD Co., Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 12
Not provided
1.Those who have been currently visiting a hospital or treated with any drug or herbal remedy for any disease 2.Those who are on diet/exercise therapy under the guidance of a doctor 3.Those who currently have or have history of severe diseases 4.Those who have serious anemia 5.Those who daily take medicine, quasi-medicine, food for specified health uses or nutritional supplements / foods on the market that have health claims related to fatigue, stress relief, cold intolerance, blood flow, blood pressure or calefacient (excluding individuals who can refrain from ingestion after receiving informed consent until the end of the study) 6.Those who currently have or have a history of drug and/or food allergies 7.Those who have donated 200 mL of the blood, including ingredient blood, within 1 months before start of the study 8.Those who have donated 400 mL of the blood within 4 months before start of the study 9.Those who joined other clinical trials within 1 month before receiving informed consent in this study, or those who are currently joining other clinical trials 10.Those who are currently pregnant, breastfeeding or planning to get pregnant during the study period. 11.Those who routinely take alcohol more than 60 g/day 12.Those who have smoked within a year 13.Those who cannot agree to abandon daily exercise from 3 days before start of food intake until end of the study 14.Those who have habits of irregular meals, or those who have irregular life rhythm such as night work or spilt shift 15.Those who are judged by the physician to be unsuitable for this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Concentration of ketone bodies
- Secondary Outcome Measures
Name Time Method Blood levels of triglycerides, total cholesterol, and LDL-cholesterol