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Efficacy evaluation of a food ingredient to skin condition in healthy adults -Randomized, double-blind, placebo-controlled, parallel-group study-

Efficacy evaluation of a food ingredient to skin condition in healthy adults -Randomized, double-blind, placebo-controlled, parallel-group study- - Efficacy evaluation of a food ingredient to skin condition

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056126
Enrollment
150
Registered
2024-11-13
Start date
2024-11-13
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

None

Interventions

Intakes of test capsules for 8 weeks Intakes of placebo capsules for 8 weeks

Sponsors

TES Holdings Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Male and Female aged from 30 to 69 years, when giving the informed consent. 2.Healthy individuals not having any chronic diseases. 3.Subjects who are concerned about decrease of moisture with skin aging. 4.Subjects who are concerned about dullness and uneven skin tone with skin aging. 5.Subjects who give the informed consents in writing, after receiving enough explanation of the purpose and details of the study, understanding the study well, and deciding to attend the study with their own will. 6.Individuals who can accomplish their tasks in the study at the appointed date. 7.Individuals who are judged suitable for this study by the investigator.

Exclusion criteria

Exclusion criteria: Subjects 1.who have some diseases with drug therapy. 2.who consecutively receive medications in the last 1 month. 3.who have severe disease histories in liver or the other tissues. 4.who have a comorbidity or disease history in respiratory system. 5.Systolic and diastolic blood pressures are over 160 mmHg and 100 mmHg, respectively. 6.who have donated over 200 or 400 mL of blood in the last 1 or 3 months. 7.who have severe anemia. 8.who could have some allergy to the test diet. 9.who are pregnant, breastfeeding, or planning to be pregnant in the near future. 10.who are alcoholic or have mental disorder. 11.who have a smoking habit. 12.who have irregular defecation. 13.who could change their life style during the study. 14.whose skin is extremely sensitive, or who have chronic ruddy complexion, outstanding pores or freckles. 15.who have some skin diseases. 16.who could have a seasonal allergy. 17.who have severe menopausal symptoms. 18.who have severe poor circulation. 19.who habitually shave their face with a razor blade. 20.who are willing to get sunburn, spend long time outdoors, during the study. 21.who habitually intake functional foods that could get skin condition better in the last 3 months. 22.who habitually consume cosmetics or foods made of microbes. 23.who routinely use pharmaceuticals that could get skin condition better. 24.who use cosmetics that could have strong effects on skin moisture or wrinkles. 25.who received a surgery on their faces or arms in the last 6 months. 26.who participated in other clinical trials in the last 3 months. 27.who and whose family work for a company manufacturing or selling healthy foods, functional foods or cosmetics. 28.who have a weakened immune system. 29.who refuse to disclose their biological sex. 30.who are judged unsuitable for this study by the investigator for other reasons.

Design outcomes

Primary

MeasureTime frame
skin moisture

Secondary

MeasureTime frame
Evaluation of skin condition Blood biochemical analysis

Countries

Japan

Contacts

Public ContactRyoma Shimizu

TES Holdings Co., Ltd Administrative Department of Clinical Trials

r.shimizu@tes-h.c.jp03-6801-8480(+81-3-6801-8480)

Outcome results

None listed

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