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A study to examine the effects of continuous intake of wasabi leaf extract powder on body composition and the skin.

A study to examine the effects of continuous intake of wasabi leaf extract powder on body composition and the skin. - A study to examine the effects of continuous intake of wasabi leaf extract powder on body composition and the skin.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000036597
Enrollment
12
Registered
2019-05-07
Start date
2019-05-17
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 adults

Interventions

Take 2 capsule containing wasabi leaf extract powder daily with a glass of cool or lukewarm water before sleep. Take 2 placebo capsule (not containing wasabi leaf extract powder) daily with a glass of

Sponsors

IMEQRD Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. 20 to 63 years old. 2. Males and females. 3. BMI 23.0 to 29.9 kg/m2 4. Smartphone users (who can input their own data into the electronic diary). 5. Those who do not intend to change or do not change everyday lifestyle habits during the study period. 6. Those who can provide their written informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who currently receive some types of drug treatment for obesity/hyperlipidemia or a drug treatment which affects lipid metabolism (except for the drugs that are taken as needed for complications/chronic diseases) 2. Those who are receiving diet therapy or exercise therapy under the direction of a physician. 3. Those who cannot stop taking health foods or supplements during the study period. 4. Those who cannot abstain from drinking the day before a test. 5. Those with a current or a past medical history of severe disease. 6. Those with a current or a past medical history of drug or food allergy. 7. Those with a current or a past medical history of drug addiction or alcoholism. 8. Those who have a metallic object present in the body as a result of surgery or other means. 9. Those who have a cardiac pacemaker or medical device implanted in the body. 10. Those who have claustrophobia. 11. Those who work the night shift on a rotating schedule. 12. Those who want to become pregnant during the study period or those who are currently pregnant or breastfeeding. 13. Those who are participating in another clinical trial or those who had been given a test drug during another clinical trial and completed another clinical trial within a month prior to the start of this study. 14. Those who were determined by the principal investigator or a sub-investigator to be unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Visceral fat area (V)

Secondary

MeasureTime frame
Subcutaneous fat area (S); V/S ratio, Weight; Body mass index (BMI); Triglycerides; Total cholesterol; High density lipoprotein cholesterol; Low density lipoprotein cholesterol; Waist circumference; Body fat percentage; Measurements of skin hydration, moisture, and elasticity

Countries

Japan

Contacts

Public ContactYoshitada Hira

IMEQRD Co., Ltd. Planning and Sales Department

clinical-trial@imeqrd.co.jp03-6704-5968

Outcome results

None listed

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