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A single-blind, faceted controlled study to evaluate the effect of multi-effect soothing repair facial cream on skin repair after medical beauty treatment

A single-blind, faceted controlled study to evaluate the effect of multi-effect soothing repair facial cream on skin repair after medical beauty treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084226
Enrollment
Unknown
Registered
2024-05-13
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Skin repair after pulsed laser and mesodermal cosmetic treatment

Interventions

Mesoderm treatment group:Subjects underwent normal care with medical dressings after mesodermal treatment, and were given either the test product or the control product on each side of the face accord
Pulsed laser therapy group:After pulsed laser treatment, subjects will apply test products on the test side and control product on the control side immediately after receiving routine care according t

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Signed the informed consent form and marked the date agreeing to participate in the study; 2) 18-60 years old, regardless of gender; 3) Willing to receive photon or water light therapy; 4) Subjects with sensitive, dry, fine lines or lack of elasticity of facial skin that researchers consider suitable for pulsed laser treatment and mesoderm treatment.

Exclusion criteria

Exclusion criteria: 1) Known history of allergies to the tested product ingredients; 2) Suffering from diseases that seriously affect wound healing; 3) Have a history of psychological and mental illness; 4) Received hydrolight or phototherapy within the first three months of enrollment; 5) Skin care products with strong efficacy, such as hydroxy acid and A-alcohol, were used within 1 month before inclusion, and the above products were used during the test; 6) Other situations where researchers believe it is not appropriate to participate in the study; 7) No other facial treatments allowed during the study period.

Design outcomes

Primary

MeasureTime frame
skin elasticity;water content;Percutaneous water loss;

Secondary

MeasureTime frame
texture;wrinkle;pores;pigment;sensitivity;Doctor score;

Countries

China

Contacts

Public ContactWang Hang

West China Stomatology Hospital, Sichuan University

614930150@gg.com+86 139 8088 8813

Outcome results

None listed

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