Healthy adult volunteers who do not have a medical condition. We exclude minors, pregnant and breastfeeding women.
Conditions
Interventions
None listed
Sponsors
FUJIFILM Corporation
Yakujihou Marketing Jimusho Co., Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: A systematic literature search is performed through scientific and clinical trial registries databases. The selection criteria are as follows. P: Healthy adult volunteers not suffering from any diseases. We will exclude minors, pregnant women, and lactating women. I: Intake the foods containing salacinol, indigestible dextrin, epigallocatechin gallate, monoglucosy lrutin, and phlorotannin. C: The control food is a placebo food that does not contain salacinol, indigestible dextrin, epigallocatechin gallate, monoglucosyl rutin, and phlorotannin. O: The primary outcome is the suppressive effect on the postprandial fat absorption
Exclusion criteria
Exclusion criteria: The literature which does not meet the key inclusion criteria will be excluded. Intervention tests without a placebo intake group are excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is postprandial triglyceride area under the curve (AUC) and RLP-C area under the curve (AUC). | — |
Countries
Japan
Contacts
Public ContactHitomi Saito
FUJIFILM Corporation Bio Science & Engineering Laboratories
Outcome results
None listed