Skincare Benefits of Kaempferol-Containing Masks

March 3, 2026 updated by: Kaohsiung Medical University Chung-Ho Memorial Hospital

Clinical Evaluation of the Skincare Benefits of Kaempferol-Containing Masks

This is an open-label, two-arm study, which will evaluate the effects of Kaempferol-containing masks on skin biophysical properties

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Taiwan
      • Kaohsiung City, Taiwan
        • Recruiting
        • Kaohsiung Medical University Chung-Ho Memorial Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Kaempferol-containing facial mask
Other: Kaempferol-containing facial mask
Kaempferol-containing facial mask
Active Comparator: Hyaluronic acid-containing facial mask
Other: Hyaluronic acid-containing facial mask
Hyaluronic acid-containing facial mask

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Skin hydration
Time Frame: 12 weeks
12 weeks
Skin transepidermal water loss
Time Frame: 12 weeks
12 weeks
Skin coloration
Time Frame: 12 weeks
12 weeks
Skin elasticity
Time Frame: 12 weeks
12 weeks
Skin wrinkles
Time Frame: 12 weeks
12 weeks
Skin pores
Time Frame: 12 weeks
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Kaohsiung Medical University Chung-Ho Memorial Hospital

Collaborators

Kaohsiung Municipal Hsiaokang Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 9, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

March 1, 2027

Study Registration Dates

First Submitted

March 3, 2026

First Submitted That Met QC Criteria

March 3, 2026

First Posted (Actual)

March 9, 2026

Study Record Updates

Last Update Posted (Actual)

March 9, 2026

Last Update Submitted That Met QC Criteria

March 3, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • S-113-20

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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