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Human biological efficacy test of recombinant mussel mucin gel

Human biological efficacy test of recombinant mussel mucin gel

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079912
Enrollment
Unknown
Registered
2024-01-16
Start date
2024-01-22
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Soothing sensitive skin

Interventions

Facial test group:There is only an experimental group on the face, without control group. Compare before and after use, and use the test product on the face. The testing time is D0, D3, and D7.
Test group(Arm):Skin injury model was created on the arm, with a total of three experimental areas. After modeling the arm injury, apply the test product to one of the test areas according to the rand
Positive control group (Arm):Skin injury model was created on the arm, with a total of three experimental areas. After modeling the arm injury, apply tacrolimus ointment to one of the experimental are
Negative control group (Arm):Skin injury model was created on the arm, with a total of three experimental areas. After modeling the arm injury, according to the random table, do not use the product in

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Age = 18 years old, = 60 years old, both male and female; 2) Good health condition; 3) The total positive score of lactate stinging test is = 3 points; 4) Willing to comply with the experimental requirements and complete the entire experiment for a total of 4 weeks, able to complete follow-up as required 5) Informed consent for the project and signing of informed consent and portrait rights consent forms

Exclusion criteria

Exclusion criteria: 1) Pregnant or lactating women; 2) Skin diseases (such as psoriasis, eczema, psoriasis, skin cancer, etc.), or obvious redness, sunburn, wounds, wear, tattoos, etc. in or near the testing area; 3) Participated in similar tests within 3 months; 4) Use any other anti allergic products within the past 3 months; 5) Participate in other clinical trial researchers; 6) Experts or professionals believe that there are other iatrogenic factors that may affect the test results.

Design outcomes

Primary

MeasureTime frame
Loss of moisture through the epidermis(Face);Current sensing threshold(Face);Blood flow perfusion volume(Face);Lactic acid stinging pain(Face);a value(Face and Arm);

Secondary

MeasureTime frame
Safety assessment(Face and Arm);

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