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A study to compare the absorbency after food intake containing plant extract for adult males (3)

A study to compare the absorbency after food intake containing plant extract for adult males (3) - A study to compare the absorbency after food intake containing plant extract (3)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000034134
Enrollment
24
Registered
2019-09-15
Start date
2018-09-18
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 adult

Interventions

Sponsors

TTC Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Healthy males aged 20-60 years

Exclusion criteria

Exclusion criteria: (1) Subjects having possibilities for emerging allergy related to the study. (2) Subjects who are under medication. (3) Subjects who are under treatment or have a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease). (4) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. (5) Subjects who constantly take in supplement richly containing licorice extract. (6) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination at the screening. (7) Subjects who have habits affecting research results, such as doing shift work day and night, or Subjects who have a plan that affect research results such as day and night shift work or going overseas. (8) Subjects who have participated in other clinical study within the last one month prior to the current study. (9) Subjects who are difficult to take the test food as instructed. (10) Subjects who donated over 200 ml of blood at least one month before the test started. (11) Subjects who have experience of bad mood or deteriorating physical condition due to blood collection. (12) Subjects who are judged as unsuitable for the study by the investigator for other reason.

Design outcomes

Primary

MeasureTime frame
AUC Cmax

Countries

Japan

Contacts

Public ContactShingo Yamamichi

TTC Co.,Ltd Clinical Research Planning Department

s.yamamichi@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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