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Comprehensive evaluation of skin condition when using facial beauty device equipped with high brightness LED and low output IPL together with beauty serum

Comprehensive evaluation of skin condition when using facial beauty device equipped with high brightness LED and low output IPL together with beauty serum: single blinded study - Comprehensive evaluation of skin condition when using facial beauty device equipped with high brightness LED and low output IPL together with beauty serum

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052550
Enrollment
12
Registered
2023-10-20
Start date
2023-10-20
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 2 items of test articles (facial device, cosmetic serum) on one side of the face for 12 weeks Use cosmetic serum on the other side for 12 weeks

Sponsors

Japan Clinical Trial Association
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Subjects with dull skin 2) Subjects with disturbed skin texture, Subjects with rough skin texture 3) Subjects whose makeup doesn't apply well 4) Subjects who have not had excessive sunburn within the past 4 weeks 5) Subjects of dry skin

Exclusion criteria

Exclusion criteria: 1.Those who are pregnant or may be pregnant, and those who are breastfeeding 2.Persons who work night shifts or day and night shifts 3.Individuals who need help from others and are unable to walk independently. 4.Subjects participating in other clinical trials 5.Factors that may affect the test results (disease such as atopic dermatitis and urticaria, inflammation, eczema, trauma, acne, tumor warts with a diameter of 5 cm or more on the cheek, etc.) , or traces of it) 6.Subjects who are judged as unsuitable for the study by the investigator for the other reason

Design outcomes

Primary

MeasureTime frame
Evaluation of devices that measure (before use, after 4 weeks, after 8 weeks, after 12 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