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A pharmacokinetic study of Food containing plant extract-Open study-

A pharmacokinetic study of Food containing plant extract-Open study- - A pharmacokinetic study of Food containing plant extract

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038596
Enrollment
10
Registered
2019-11-16
Start date
2019-11-18
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

Single ingestion of test food (low dose) Single ingestion of test food (high dose)

Sponsors

KSO Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Healthy males and females aged 20 to 64 years-old. (2)Subjects who can make self-judgment and are voluntarily giving written informed consent.

Exclusion criteria

Exclusion criteria: (1)Subjects who are judged as unsuitable for the current study by the investigator through the screening tests. (2)Subjects who are diagnosed as anemic and not suitable for frequent collection of blood. (3)Subjects who take medications. (4)Subjects who regularly take functional foods (including Food for Specified Health Uses or Foods with Function Claims). (5)Subjects who have declared allergic reaction to ingredients of test foods. (6)Subjects who contract or are under treatment for serious diseases (e.g., kidney disease, heart disease, respiratory disease, endocrine disease, and/or metabolic disease). (7)Subjects who have a chronic disease and use medications continuously. (8)Subjects who have a history and/or a surgical history of digestive disease affecting digestion and absorption. (9)Subjects who have had diarrhea within the last one week prior to the screening tests and/or who are prone to diarrhea. (10)Subjects who have donated over 200 mL of blood and/or blood components within the last one month prior to the current study or over 400 mL of blood and/or blood components within the last three months prior to the current study. (11)Subjects who have a history of and/or contract drug addiction and/or alcoholism. (12)Subjects who are planning to participate and/or had participated in other clinical studies within the last one month prior to the current study. (13)Subjects who are planning to become pregnant after informed consent for the current study, pregnant or lactating. (14)Subjects who are judged as unsuitable for the current study by the investigator for other reasons.

Design outcomes

Primary

MeasureTime frame
Plasma concentration of plant extract-derived component

Countries

Japan

Contacts

Public ContactYoshika Komori

KSO Co., Ltd Sales Department

yoshi@kso.co.jp0334527733

Outcome results

None listed

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