Recruiting NCT07458334
Skincare Benefits of Kaempferol-Containing Masks
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Kaempferol-containing facial mask, Hyaluronic acid-containing facial mask.
- Who it may be relevant to
- Registry conditions: Skin Biophysical Properties. Basic parameters: 25 years — 60 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Taiwan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Clinical Evaluation of the Skincare Benefits of Kaempferol-Containing Masks
Overview
This is an open-label, two-arm study, which will evaluate the effects of Kaempferol-containing masks on skin biophysical properties
Interventions
- Other Kaempferol-containing facial mask
Kaempferol-containing facial mask - Other Hyaluronic acid-containing facial mask
Hyaluronic acid-containing facial mask
Primary outcome measures
- Skin hydration [Time frame: 12 weeks]
- Skin transepidermal water loss [Time frame: 12 weeks]
- Skin coloration [Time frame: 12 weeks]
- Skin elasticity [Time frame: 12 weeks]
- Skin wrinkles [Time frame: 12 weeks]
- Skin pores [Time frame: 12 weeks]
Eligibility criteria
Inclusion criteria
- Female subjects between 25 and 60 years old
Exclusion criteria
- Pregnant or breastfeeding women
- Subjects who are allergic to the product
- Subjects with psoriasis or atopic dermatitis
- Subjects who have taken systemic corticosteroids within 2 weeks
- Subjects who have taken oral retinoid within 1 week
- Subjects with severe medical conditions, such as cardiovascular, liver, kidney, or hematopoietic system disorders
- Subjects with tuberculosis
- Subjects with viral hepatitis or other infectious diseases
- Subjects with psychiatric disorders
- Subjects with external trauma or infections
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Taiwan · 1 center
- Kaohsiung Medical University Chung-Ho Memorial Hospital — Kaohsiung City
Identifiers
NCT: NCT07458334 · S-113-20