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

Not Applicable

• Conditions: Healthy adult Female

• Registration Number: JPRN-UMIN000051005
• Lead Sponsor: Japan Clinical Trial Association

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-05-09
• Study Completion: 2023-07-04
• Last Update Posted: 20 November 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: Female
• Target Recruitment: 14

Inclusion Criteria

Not provided

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Measuring equipment evaluation (before use, after 4 weeks, after 8 weeks)

Secondary Outcome Measures

Name	Time	Method
subjective assessment