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Exploratory Study on the Efficacy and Safety of Jmoon Transdermal Collagen Light Beauty Device on Facial Anti-aging

Exploratory Study on the Efficacy and Safety of Jmoon Transdermal Collagen Light Beauty Device on Facial Anti-aging

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090845
Enrollment
Unknown
Registered
2024-10-14
Start date
2024-07-08
Completion date
Unknown
Last updated
2024-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Facial Aging

Interventions

The test group:Jmoon Transdermal Collagen Light Beauty Device, used once daily for 4 weeks

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1.Females aged 25-50 years (inclusive of 25 and 50 years). 2.Mild to moderate facial aging, lack of elasticity, rough and dull skin (refer to the skin aging scale). 3.Facial crow's feet, under-eye wrinkles, forehead lines, nasolabial folds, and glabellar lines. 4.No cosmetic procedures such as laser chemical peels within the past 3 months before the test. 5.Voluntarily participate in the test and sign the informed consent, maintaining original lifestyle during the test. 6.Able to comply with and participate in follow-up visits, adhere to daily photo check-ins, and promptly report any changes in health status or adverse reactions during the test. 7.Avoid excessive sun exposure during the test period

Exclusion criteria

Exclusion criteria: 1.Women who are pregnant, lactating, or intending to conceive. 2.Individuals with photosensitivity/scar constitution. 3.Patients currently participating in other clinical trials. 4.Patients with wounds, epidermal rupture, herpes/folliculitis at the test site. 5.Individuals whose test sites have scars, pigmentation, atrophy, port wine stains, or 6.other imperfections that affect the judgment of test results. 7.Patients with diabetes, tumors, asthma, autoimmune diseases, or other severe organic or mental diseases. Individuals who have taken oral antihistamines within the past week, applied any anti-inflammatory drugs to the test site within the past two months, or used retinoids, alpha hydroxy acids, salicylic acid, hydroquinone, etc., within the past three months.

Design outcomes

Primary

MeasureTime frame
Facial spots, texture, pores, and wrinkles;Facial stratum corneum hydration, sebum content, skin elasticity, firmness, glossiness;Facial dermal thickness and density;

Secondary

MeasureTime frame
Participant satisfaction score;

Countries

China

Contacts

Public ContactWei Fang

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

Weifang081782@163.com+86 136 3660 2969

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026