New serum promises glowing skin in just 4 weeks
NCT ID NCT07200635
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This 4-week study tested a test serum, used alone or with hyaluronic acid injections, in 90 healthy Chinese women aged 25-40. The goal was to see if the serum improves skin hydration, elasticity, and reduces redness. Researchers measured skin changes with special devices and questionnaires.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- facial serum and hyaluronic acid injection
- What this could lead to
- If it works, this could point toward a simple serum or combination treatment for improving skin hydration and reducing redness.
- What could go wrong
- This is a small, short-term study in healthy women only, so results may not apply to others. The serum is cosmetic, not a medical treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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90 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Sep 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 to 40 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Chinese female with 25-40 years old. 2. All skin types by subjects' self-perceived. 3. Willing to perform HA injection. 4. Did not perform any of the beauty procedure projects in the past 6 months. 5. Lack of hydration, radiance, brightness, smoothness, firmness and elasticity by self-claimed. 6. Presenting with corresponding severity for the attribute evaluated by Dermatologist included: * Radiance, smoothness, elasticity, cheek plumpness and firmness: 3≤grade≤6. * Global fine lines: 3≤grade. * Underneath eye wrinkles: 2≤grade≤5. * Forehead wrinkles: 1\<grade≤4. * Glabella wrinkles: 1\<grade. 7. All accept not to use any cosmetics, skincare products, beauty equipment, all topical medications and cleansing products on face at visit days. 8. Did not participate any clinical test or cosmetic product test on skin within 1 months. 9. No disagreement of dermatologist because of other reasons that exclude the participation of the volunteer. 10. In general, good health at the time of the study. 11. Willing and able to participate as evidenced by signing of informed consent \& photo release form. 12. Must be willing to comply with all study protocol requirements. Exclusion Criteria: 1. Pregnant or breast-feeding woman or woman planning pregnancy during the study. 2. Subject deprived of rights by a court or administrative order. 3. Major subject to a guardianship order. 4. Subject residing in a health or social care establishment. 5. Patient in an emergency setting. 6. Subject with a skin disease in the test areas as well as skin allergy (particularly e.g., acne, rosacea, eczema). 7. Subject presenting a stable or progressive serious disease (per investigator's assessment). 8. Immuno-compromised subject. 9. Subject with history of allergy to cosmetic or personal care products or ingredients. 10. Subject presenting excessive exposure to sunlight or UV radiation (investigator's assessment). 11. Subject with history of sunlight sensitivity or allergies. 12. Subject regularly practicing aquatic or nautical sports. 13. Subject regularly attending a sauna. 14. Subject with physical highly sensitive constitution. 15. Subject with cardiovascular or circulatory history. 16. Subject with a history of skin cancer or malignant melanoma. 17. Intake of antihistamines, antibiotics, corticosteroids, non-steroidal anti-inflammatories or immune-suppressants in the last 6 months before study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Shanghai China-norm Quality Technical Service Co., Ltd.
Shanghai, Shanghai Municipality, 200072, China
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Other studies related to the condition(s) this trial covers.