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Effect of Powdered food on a Condition of Skin in Healthy Adult Females.

Effect of Powdered food on a Condition of Skin in Healthy Adult Females. - Effect of Powdered food on a Condition of Skin.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029644
Enrollment
40
Registered
2019-04-01
Start date
2018-01-16
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

To explore the effect of powdered food supplementation on skin.

Interventions

Duration: 8weeks. Test materials: Powdered food. Does: 2 portions per day. Duration: 8weeks. Test materials: Powdered placebo food. Does: 2 portions per day.

Sponsors

MORINAGA & CO.,Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Healthy postmenopausal subjects from 55 to 65 years old. 2.BMI is >= 18.5 kg/m^2 and < 25.0 kg/m^2. 3.Subjects who concern with rough skin. 4.Subjects who keep regular daily life and sleep as possible. 5.Subjects who can visit the examination place on a fixed schedule. 6.Subjects who can cooperate with weight measurement, a questionnaire and skin measurement at the examination place. 7.Subjects who can intake test food dissolved with hot water etc., twice a day during the examination. 8.Subjects who can fill up the examination record everyday.

Exclusion criteria

Exclusion criteria: 1.Subjects who have food allergy. Especially subjects who are sensitive to gelatin. 2.Subjects who have possibility of hay fever. 3.Subjects who have been medical history of physical disorder when they took supplements. 4.Subjects who are diabetes or hypercholesterolemia. 5.Subjects who take medicine and/or food for specified health use. 6.Subjects who took supplements and/or drink for improvement of skin condition within 1 month. 7.Subjects who smoke. 8.Subjects who had laser treatment and/or peeling treatment within 1 year. 9.Subjects who regularly have beauty treatment or plan to have beauty treatment. 10.Subjects who have possibility of excessive sunburn.

Design outcomes

Primary

MeasureTime frame
Measurement of skin condition. (measurement time: 0, 4, 8 weeks after intervention)

Secondary

MeasureTime frame
Measurement of visual analog scale. (measurement time: 0, 4, 8 weeks after intervention)

Countries

Japan

Contacts

Public ContactInagaki, Hiroyuki

MORINAGA & CO.,Ltd. Research Institute

h-inagaki-jj@morinaga.co.jp045-571-2504

Outcome results

None listed

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