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Effects on Face and Body When Using Professional Equipment Designed for Esthetic Salons

Effects on Face and Body When Using Professional Equipment Designed for Esthetic Salons: single blinded study - Effects on Face and Body When Using Professional Equipment Designed for Esthetic Salons

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000053554
Enrollment
18
Registered
2024-02-07
Start date
2024-02-07
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

Interventions

Receive treatment on only one side of the face and body once a week for 4 weeks continuously The other side of the face and body, no using test article

Sponsors

Japan Clinical Trial Association
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Subjects with BMI of 25 or more and less than 30 2.Subjects who are concerned about dry or sagging skin

Exclusion criteria

Exclusion criteria: 1. Subjects who have a daily exercise routine and training 2. Subjects who are not comfortable with the tingling sensation of facial equipment, etc. 3. Subjects who are pregnant, lactating, or wish to become pregnant during the study period 4. Subjects who are taking medicines that may affect the study (e.g. slimming or cellulite removal) 5. Subjects are taking or will start taking health food products that may affect the study 6. Subjects are undergoing treatment (hormone replacement therapy, drug therapy, or other) at a medical institution for the treatment or prevention of disease, or whose condition is judged to be in need of treatment at the time consent is obtained. 7. Subjects have participated in any other human studies (all human studies using cosmetics, foods, pharmaceuticals, quasi-drugs, medical devices, etc.) within the past 4 weeks, or Subjects are scheduled to participate in any other human studies during the period when this study is scheduled to be conducted. 8. Other subjects deemed inappropriate by the study investigator.

Design outcomes

Primary

MeasureTime frame
Evaluation of devices that measure (Before use / 4 weeks later)

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