A 56-Day Exploratory Study of NatureU® Mind Care BeautyU Caps on Skin Aging Parameters
NUAA
A 56-Day Single-Arm Exploratory Study of NatureU® Mind Care BeautyU Caps on Crow's-Feet Wrinkle Count, Skin Hydration, and Related Skin-Aging Parameters in Adult Women
1 other identifier
interventional
31
1 country
1
Brief Summary
This was a 56-day, single-center, open-label, single-arm exploratory study evaluating within-participant changes in skin-aging parameters after daily oral intake of NatureU® Mind Care BeautyU Caps in adult women. Participants took one capsule daily for 56 days. The primary outcome was change from baseline in crow's-feet wrinkle count at Day 56 assessed by PRIMOS CR imaging. The secondary outcome was change from baseline in stratum corneum hydration at Day 56 assessed by Corneometer CM 825. Additional exploratory outcomes included other wrinkle topography parameters, skin elasticity, radiance, pigmentation, pore-related parameters, dermal thickness and density, and participant-reported skin appearance outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 11, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 8, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 8, 2025
CompletedFirst Submitted
Initial submission to the registry
April 30, 2026
CompletedFirst Posted
Study publicly available on registry
May 6, 2026
CompletedMay 11, 2026
May 1, 2026
2 months
April 30, 2026
May 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change From Baseline in Crow's-Feet Wrinkle Count at Day 56
Crow's-feet wrinkle count was assessed using PRIMOS CR imaging. The primary endpoint was the within-participant change from baseline to Day 56.
Baseline and Day 56
Secondary Outcomes (1)
Change From Baseline in Stratum Corneum Hydration at Day 56
Baseline and Day 56
Other Outcomes (1)
Change From Baseline in Additional Wrinkle Topography Parameters at Day 28 and Day 56
Day 28, Day 56
Study Arms (1)
NatureU® Mind Care BeautyU Caps
EXPERIMENTALParticipants received NatureU® Mind Care BeautyU Caps, one capsule orally once daily for 56 days.
Interventions
An oral nutricosmetic supplement containing PQQ, quercetin, ergothioneine, cranberry polyphenols, and related formulation components. Participants took one capsule daily for 56 days.
Eligibility Criteria
You may qualify if:
- Adult woman aged 36 to 56 years, inclusive.
- Healthy participant as judged by the investigator.
- Cheek skin hydration below 60 C.U.
- Visible crow's-feet wrinkles.
- Facial laxity or reduced facial radiance.
- At least one visible facial spot meeting the prespecified size and ITA value criteria.
- Willing to take the study product once daily for 56 consecutive days.
- Willing to complete scheduled skin assessments at baseline, Day 28, and Day 56.
- Willing to maintain regular lifestyle habits during the study period.
- Willing to avoid confounding skincare products, cosmetic procedures, medications, and health products during the study period.
- Provided written informed consent before any study-related procedure.
You may not qualify if:
- Skin condition that could interfere with study assessments.
- Highly allergic constitution.
- Known allergy or intolerance to any ingredient of the study product.
- Pregnant or lactating.
- Planned pregnancy during the study period.
- Severe systemic illness.
- Serious psychiatric disorder.
- Serious endocrine disorder.
- Recent participation in another clinical study.
- Recent use of products or procedures that could influence skin outcomes.
- Use of other oral or topical products that could interfere with skin-aging assessments during the study period.
- Recent cosmetic dermatology procedures or treatments that could affect the target assessment areas.
- Inability to comply with study procedures.
- Any condition judged by the investigator to make participation inappropriate.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CTI AiPu Medical Laboratory (Shanghai) Co., Ltd
Shanghai, Shanghai Municipality, 200040, China
Study Officials
- STUDY DIRECTOR
Luke Law, Dr
OmniSolutions Laboratory Holdings Limited
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 30, 2026
First Posted
May 6, 2026
Study Start
January 11, 2025
Primary Completion
March 8, 2025
Study Completion
March 8, 2025
Last Updated
May 11, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to privacy protection and ethical considerations.