Healthy adults
Conditions
Interventions
None listed
Sponsors
KAGOME CO., LTD.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (PICOS) Participant: Healthy adults without illness (excluding pregnant women, women who plan to become pregnant and lactating women) Intervention: Oral intake of test food containing lycopene (regardless of the form and amount of intake) Comparison: Oral intake of test food without lycopene, or no intervention Outcome measurement: Blood LDL-C level Study design: Randomized controlled parallel trials (RCT-P), randomized controlled crossover trials (RCT-C), quasi-randomized controlled parallel trials (qRCT-P), quasi randomized controlled crossover trials (qRCT-C), non-randomized controlled parallel trials (nonRCT-P), non-randomized controlled crossover trials (nonRCT-C), and non-randomized controlled trials (Language) Eligibility is not restricted by language
Exclusion criteria
Exclusion criteria: Exclude studies that did not aim to evaluate blood lipids, proceedings and unpublished studies which don't give us enough research details, and other gray documents that are difficult to verify
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood LDL-C level | — |
Countries
Japan
Contacts
Public ContactYuichiro Nakazawa
KAGOME CO., LTD. Diet and Well-being Research Institute
Outcome results
None listed