Skip to content

Clinical observation on efficacy and safety of tea leavened retinol elastic and light lines essence

Clinical observation on efficacy and safety of tea leavened retinol elastic and light lines essence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083160
Enrollment
Unknown
Registered
2024-04-17
Start date
2024-05-06
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

wrinkle

Interventions

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) 50-65 years old, female; 2) Has obvious crow's feet; 3) Skin dullness; 4) Skin is relatively loose; 5) Willing to comply with the experimental requirements and complete the entire experiment for a total of 84 days.

Exclusion criteria

Exclusion criteria: 1) Planned pregnancy or pregnant and lactating women; 2) Has allergic diseases and a history of allergies to cosmetics, skincare products, and other topical preparations; 3) Skin diseases (such as psoriasis, eczema, psoriasis, skin cancer, etc.), or obvious wounds, abrasions, tattoos, scars, pigmentation, atrophy, bright red nevi, or other defects in or near the test area; 4) Participate in other clinical trial researchers; 5) Any other circumstances that the researcher deems unsuitable for participation in the trial.

Design outcomes

Primary

MeasureTime frame
wrinkle;Skin roughness;Skin color;Security assessment;

Secondary

MeasureTime frame
Skin elasticity;Skin glossiness;

Countries

China

Contacts

Public ContactWang Xi

West China Hospital, Sichuan University

xierwang@126.com+86 28 8542 2075

Outcome results

None listed

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