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A study for the effect of the intake of a plant extracts containing drink on condition of skin.

A study for the effect of the intake of a plant extracts containing drink on condition of skin. - A study for the effect of the intake of a plant extracts containing drink on condition of skin.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038368
Enrollment
40
Registered
2019-10-28
Start date
2019-10-28
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

Oral intake of placebo drink for 4 weeks Oral intake of active drink for 4 weeks

Sponsors

Inforward Inc.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Healthy female aged from 20 to 39 years old 2. Subjects who have a dry skin trouble in arm. 3. Subjects who has atopic disposition, but they are not diagnosed as atopic dermatitis 4. Menstrual cycle is stable 5. Subjects who can forbid intaking supplements.

Exclusion criteria

Exclusion criteria: 1. Subjects who have been suffered from bronchial asthma, allergic rhinitis, conjunctivitis, and atopic dermatitis 2. Subjects who have the rash resulting from psoriasis or skin allergy 3. Subjects who are outpatients or were treated by doctor recently. 4. Subjects who are using external preparations and/or moisturizer for face, cubital fossa, forearm, popliteal space, leg and neck 5. Subjects who take medicine 6. Subjects who have skin disorder, suntan, abrasion and tattoo in face, cubital fossa, forearm, popliteal space, leg and neck 7. Subjects who have received or forbid cosmetic medicine in face, cubital fossa, lower arm, popliteal space, leg and neck 8. Subjects who have possibilities for emerging allergy to foods and drugs. 9. Subjects who are pregnant or lactating, or planned to become pregnant in the near future. 10. Current smoker 11. Subjects who are participate in the other clinical studies 12. Subjects who are judged as unsuitable for the study by the investigator for other reason.

Design outcomes

Primary

MeasureTime frame
Evaluation by a questionnaire (measurement time: 0, 2, 4, 5weeks after ingestion of the test drink)

Secondary

MeasureTime frame
Measurement of skin condition (measurement time: 0, 2, 4weeks after ingestion of the test drink)

Countries

Japan

Contacts

Public ContactKanako Sakurai

INFORWARDinc. EBISU Skin research center

sakurai@inforward.co.jp81-3-5793-8712

Outcome results

None listed

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