Effects of test food on lipid metabolism

Not Applicable

• Conditions: Healthy adults

• Registration Number: JPRN-UMIN000041607
• Lead Sponsor: Morinaga & Co., Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-09-15
• Study Completion: 2020-12-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

Not provided

Exclusion Criteria

1) Individuals who take foods more than three times a week with functional claims or foods or supplements containing Passienol-TM now or in the past 1 month, or will take them for this test period. 2) Individuals who take medications more than three times a week now or in the past 1 month, or will take them for this test period. 3) Individuals who take food for specified health use or foods with functional claims or supplements claiming to improve lipid metabolism more than three times a week now or in the past 1 month, or will take them for this test period. 4) Individuals who are allergic to especially foods or medicines or rubber. 5) Individuals who have currently or a history of hepatopathy, kidney damage, heart disease, lung, and gastrointestinal disease. 6) Individuals who were hospitalized in the past 6 months, or will be hospitalized for this test period. 7) Individuals who are currently treating anemia. 8) Individuals who are expected to have severe menstrual pain at one of the three cycle ergometer tests. 9) Females who are or are possibly pregnant, or are lactating. 10) Individuals who are a smoker. 11) Individuals who are heavy drinker of alcohol. 12) Individuals who have irregular life rhythms such as shift workers and late-night workers. 13) Individuals who participated in other clinical studies in the past 4 weeks, or will participate for this test period. 14) Individuals who donated total more than 200mL whole blood or blood component for the past 1 month. 15) Males who donated total more than 400mL whole blood for the past 3 months. 16) Females who donated total more than 400mL whole blood for the past 4 months. 17) Males who will donate total more than 1200mL blood for the past 12 months and this test period. 18) Females who will donate total more than 1200mL blood for the past 8 months and this test period. 19) Individuals judged inappropriate for this study by the principal investigator.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Expired-gas measurement (lipid oxidation, carbohydrate oxidation, respiratory quotient)

Secondary Outcome Measures

Name	Time	Method
Serum free fatty acid concentration, pulse rate (oxidative stress-antioxidant potential, concentration of serum lipid metabolites and hormones, oxygen consumption, and serum T-cho, LDL-Cho, HDL-Cho, TG and Glucose concentration)