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Study on the efficacy and safety of the facial massage device on skin in healthy subjects

Study on the efficacy and safety of the facial massage device on skin in healthy subjects - Study on the efficacy and safety of the facial massage device on skin in healthy subjects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000050696
Enrollment
23
Registered
2023-03-28
Start date
2023-03-28
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 people

Interventions

For 8 weeks, a facial massage device and basic cosmetics are used on the right side of the face. Use only basic cosmetics on the left face for 8 weeks.

Sponsors

university of tokyo
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Not currently using a facial massage device (2) Women of normal health between the ages of 20 and 60 (3) Able to practice the instructed usage by themselves. (4) No other beauty device treatment must be performed on the face. (5) Able to make hospital visits in accordance with the research schedule. (6) The subject must have received a thorough explanation of his/her participation in this study, and must have given written consent of his/her own free will based on a thorough understanding of the subject's situation.

Exclusion criteria

Exclusion criteria: Persons who meet at least one of the following exclusion criteria are excluded. (1) Patients who have experienced hypersensitivity or contact dermatitis to materials used in facial massage products. (2) Persons who have experienced hypersensitivity or contact dermatitis to ingredients contained in basic cosmetics to be used in combination with the product. (3) Patients with inflammation or scars on the face. (4) Pregnant or nursing mothers. (5) Patients with malignant tumors (except in cases where the tumor has been cured by surgery, etc.) (6) Persons with significantly different skin conditions or symptoms on both sides of the face (7) Any other person who is deemed inappropriate as a research subject by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Changes in skin elasticity at 4 and 8 weeks of initiation

Countries

Japan

Contacts

Public ContactJun Omatsu

The university of tokyo hospital dermatology

omatsuj-der@h.u-tokyo.ac.jp0338155411

Outcome results

None listed

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