Skip to content

A randomized controlled trial for improving effects of test food on skins in women

A randomized controlled trial for improving effects of test food on skins in women - A randomized controlled trial for improving effects of test food on skins in women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015327
Enrollment
48
Registered
2014-10-03
Start date
2014-10-03
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

Duration: 12 weeks Test material: test food 1 capsules per day (258mg/day) Duration: 12 weeks Test material: Placebo 1 capsules per day (258mg/day)

Sponsors

CPCC Co.,Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1)Females aged 30 to 64 years old (2)Written informed is required

Exclusion criteria

Exclusion criteria: (1)These prescreened medicine. (2)These having Food for Specified Health Uses (FOSHU) and/or health food. (3)Subjects who have previous medical history and/or current medical history of serious diseases (e.g., heart, liver, kidney and/or digestive organ). (4)Pregnant women, lactating women, or women who want to get pregnant during the trial period (5)Heavy alcohol drinker. (6)Those that have extremely disheveled lifestyle and/or dietary habits. (7)Subjects who have previous medical history of drug and/or food allergy. (8)Subjects who have skin allergy such as the atopy. (9)Subjects with more than of number of cigarettes smoked an average of 21 per day (10)Subjects who have been participated in another trial or other investigational and/or enrolled in the other clinical trials within about last 1 month. (11)Subjects who have treated cosmetic care(e.g., electric facials, esthetic, peeling and/or laser medical treatment). (12)Subjects who have donated over 200 mL of blood and/or blood components within the last one month prior to the current study. (13)Subjects who have donated over 400 mL of blood and/or blood components within the last four months prior to the current study. (14)Subjects who collected blood amount of blood sampling over 800 mL within the last twelve months prior to the current study and this clinical trial's blood sampling. (15)Subjects who have been determined ineligible by principal investigator or sub-investigator.

Design outcomes

Primary

MeasureTime frame
Moisture content of the stratum corneum Skin elasticity

Secondary

MeasureTime frame
transepidermal water loss erythema total area of wrinkle skin texture Analysis of stains, wrinkles, pores, skin color, hidden stains using VISIA Questionnaires(VAS)

Countries

Japan

Contacts

Public ContactMasanori Numa

CPCC Co.,Ltd. Plan Sales Department

cpcc-contact@cpcc.co.jp03-5297-3112

Outcome results

None listed

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