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Effect on the area around the eyes by continuous use of the EMS facial device for the eyes

Effect on the area around the eyes by continuous use of the EMS facial device for the eyes: single blinded study - Effect on the area around the eyes by continuous use of the EMS facial device for the eyes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051005
Enrollment
24
Registered
2023-05-09
Start date
2023-05-09
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 Female

Interventions

Use facial device and 2 types of test cosmetics for 8 weeks No device, only 2 cosmetics

Sponsors

Japan Clinical Trial Association
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Subjects with a BMI value of 22-23

Exclusion criteria

Exclusion criteria: 1. Subjects who have a smoking habit 2.Subjects who have a history of serious liver disorder, renal disorder, or heart disease 3. Subjects who have 5 or more metal objects (bolts, silver teeth, etc.) for maxillary treatment 4. Subjects who have a history of other serious diseases 5. Subjects who are currently going to the hospital for some kind of disease 6.Subjects who have received treatment such as immunosuppression within the past 3 months 7.Subjects who may have an allergic reaction to the test product ingredients 8. Subjects with chronic skin diseases such as atopic dermatitis 9. Subjects who have scars, warts, pimples, permanent makeup, burns, etc. that affect the evaluation measurement on the face 10. Subjects with claustrophobia 11. Subjects who are receiving "hormone replacement therapy" 12.Subjects who have experience of aesthetic medicine that may affect the test site 13.Subjects who use supplements such as amino acids and proteins on a daily basis 14. Subjects who have difficulty maintaining lifestyle habits (eating, exercising, sleeping, skin care, etc.) 15. Subjects who drink excessively (e.g. 500ml of beer, 1 go of sake (180ml), 2 glasses of wine (200ml) or more) 16. Subjects who have difficulty filling in the subject diary 17.Subjects who are pregnant, breastfeeding, or may be pregnant 18.Subjects who have participating in other clinical trials at the start of this trial 19. Individuals or family members who work for a company that develops, manufactures, or sells beauty equipment or supplements

Design outcomes

Primary

MeasureTime frame
Measuring equipment evaluation (before use, after 4 weeks, after 8 weeks)

Secondary

MeasureTime frame
subjective assessment

Countries

Japan

Contacts

Public ContactTakeshi Kaneko

Japan Clinical Trial Association N.A.

info@yakujihou.org0364574666

Outcome results

None listed

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