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Efficacy Test of a Moisturizing and Anti-aging Facial Mask

Efficacy Test of a Moisturizing and Anti-aging Facial Mask for Skin Improvement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07622160
Enrollment
60
Registered
2026-06-03
Start date
2026-04-29
Completion date
2026-07-31
Last updated
2026-06-03

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

Conditions

Anti Skin Aging, Skin Condition, Skin Hydration

Keywords

Facial mask, Skin hydration, Anti skin aging, Skin soothing

Brief summary

The objective of this study is to evaluate the effect of Moisturizing facial mask and Anti-aging facial mask on human skin condition improvement.

Detailed description

This study is a single-center, self-controlled human trial designed to evaluate the skin beauty effect of Moisturizing facial mask and Anti-aging facial mask. Healthy adult participants aged above 18 years will be enrolled. Participants will be informed to apply the facial mask on whole face three times per week for 4 consecutive weeks. Skin measurement and self-assessment questionnaires will be conducted at baseline (before intake), after single use, and after continuous use for 2 and 4 weeks.

Interventions

OTHERHydrating Repairing Mask

Applying the facial mask three times per week for a continuous period of 4 weeks

OTHERAnti-aging Rejuvenating Mask

Applying the facial mask three times per week for a continuous period of 4 weeks

Sponsors

TCI Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Participants aged 18 years or older

Exclusion criteria

* Non-voluntary participants. * Individuals diagnosed by a physician with skin diseases, liver cirrhosis, or chronic renal failure. * Individuals with known allergies to cosmetics, medications, or foods. * Pregnant or breastfeeding individuals. * Individuals taking medications for chronic diseases. * Students taught or supervised by the principal investigator.

Design outcomes

Primary

MeasureTime frameDescription
The change of skin hydrationChange from Baseline skin hydration at 4 weeksCorneometer® CM825 (CK, Germany) was utilized to measure skin surface hydation. Units: arbitrary Corneometer® units 0-120.
The change of skin rednessChange from Baseline skin redness at 4 weeksChroma Meter MM500 was utilized to measure face skin redness. Units: a\* value
The change of skin textureChange from Baseline skin texture at 4 weeksVISIA Complexion Analysis was utilized to measure skin texture. Units: arbitrary units
The change of skin wrinklesChange from Baseline skin wrinkles at 4 weeksVISIA Complexion Analysis was utilized to measure skin wrinkles. Units: arbitrary units

Secondary

MeasureTime frameDescription
The change of transepidermal water loss (TEWL)Change from Baseline TEWL at 4 weeksTewameter® TM300 (CK, Germany) was utilized to measure TEWL. Units: g/hm²
The change of skin toneChange from Baseline skin tone at 4 weeksChroma Meter MM500 was utilized to measure face skin tone. Units: Individual Typology Angle (ITA°)
The change of skin poresChange from Baseline skin pores at 4 weeksVISIA Complexion Analysis was utilized to measure skin pores. Units: arbitrary units
The change of skin elasticityChange from Baseline skin elasticity at 4 weeksSkin elasticity (Softplus, Italy) was utilized to measure face skin elasticity. Units: arbitrary units
The change of skin collagen densityChange from Baseline skin collagen density at 4 weeksDermaLab® Series SkinLab Combo was utilized to measure skin collagen density. Units: arbitrary units

Countries

Taiwan

Contacts

PRINCIPAL_INVESTIGATORChia-Hua Liang, Ph.D.

Chia Nan University of Pharmacy & Science

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026