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Efficacy test of supplement containing plant extract

Efficacy test of supplement containing plant extract - Efficacy test of supplement containing plant extract

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000036773
Enrollment
40
Registered
2020-05-15
Start date
2019-05-08
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Japanese adult

Interventions

Sponsors

KYOWA TRIAL CO., LTD
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Persons aged 20 to 65 years of age at the time of obtaining informed consent 2) A healthy person who is not currently treating any disease 3) Persons with BMI of 25.0 kg / m2 or more and less than 30.0 kg / m2 at screening 4) Persons with a VFA of 80 cm2 or more using a CT scanner system 5) Those who can visit the designated medical institution on the scheduled examination date 6) A person who agreed in writing after fully understanding the purpose and content of this study

Exclusion criteria

Exclusion criteria: 1)Those who have difficulty participating in the study due to liver, kidney, heart disease, respi ratory disorder, endocrine disorder, metabolic disorder, neurological disorder, consciousness disorder, diabetes (according to the criteria establ ished by the Japan Diabetes Association), and o ther diseases 2) Person with a history of cardiovascular disease 3) Those who are taking glucose metabolism, lipid metabolism, blood pressure improvement drugs 4) Those who regularly use medicines and health foods / supplements (including foods for specified health, functional labeling foods and nutritionally functional foods) that may affect this study (but stop taking it at the time of obtaining consent) The person who can do it does not correspond) 5) Persons who have allergies related to the test food 6) Those who have experienced poor mood or physical condition by blood collection in the past 7) Those who donated more than 200 mL from the month before the start of the test to the start of the test 8) Those who are participating in other clinical trials or within 4 weeks after the trial 9) Alcoholic drinkers and excessive smokers 10) Eating habits are extremely irregular 11) Those who wish to become pregnant during the study period, pregnant women (including those who may be pregnant) or those who are lact ating 12) Those who can not agree with the purpose of the description of this exam that is conducted in advance In addition, those who were judged inappropriate for this study by the study investigator

Design outcomes

Primary

MeasureTime frame
Body fat percentage and change Neutral fat and change

Secondary

MeasureTime frame
Weight and change BMI and change Waist circumference and change Hip circumference and amount of change

Countries

Japan

Contacts

Public ContactMegumi Takahashi

RYUSENDO CO., LTD Development Office

m.takahashi@ryusendo.co.jp03-3985-8346

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026