Clinical evaluation of the safety and effectiveness of the nanofiber undereye pad to improve surface wrinkles and dark circles under the eyes
Phase 2
Recruiting
- Conditions
- periorbital wrinkle, dark circle and puffiness.Changes in skin textureR23.4
- Registration Number
- IRCT20210130050179N9
- Lead Sponsor
- ano tarpak company
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Male or female aged 18-59 years
Signed informed consent knowingly
The presence of mild to moderate periorbital wrinkle and darkness
Exclusion Criteria
Using any eye product within 2 weeks before the intervention
Strict diet in the period of 2 weeks before the intervention
Pregnancy or lactation
Being exposed to strong sunlight during the day
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of under eye dark circle and wrinkle. Timepoint: Before intervention and 6 and 28 days after treatment. Method of measurement: Based on GIAS(Global Aesthetic Improvement Scale).
- Secondary Outcome Measures
Name Time Method Melanin content. Timepoint: fore intervention and 6 and 28 days after treatment. Method of measurement: Mexameter.;Infra-orbital pigmentation severity and degree of lightness. Timepoint: fore intervention and 6 and 28 days after treatment. Method of measurement: Visioface.