BeauSaki Bird's Nest Peptide Efficacy
Efficacy Evaluation of BeauSaki Edible Bird's Best Peptide Product
1 other identifier
interventional
40
1 country
1
Brief Summary
The goal of this clinical trial is to learn whether BeauSaki Edible Bird's Nest Peptide Product can improve facial skin conditions in healthy adult participants. The main questions it aims to answer are: Can daily intake of the edible bird's nest peptide product improve facial skin hydration, elasticity, brightness, wrinkles, pores, spots, redness, and skin texture after 8 weeks? Is the edible bird's nest peptide product well tolerated by participants during the study period? Researchers will compare participants who take the edible bird's nest peptide capsule with participants who take a placebo capsule without edible bird's nest to see if the product improves facial skin conditions. Participants will:
- Take one capsule daily for 8 weeks.
- Visit the study site at baseline, week 4, and week 8 for non-invasive facial skin assessments.
- Cleanse their face with water and rest under room temperature conditions for 30 minutes before each skin assessment.
- Complete a brief questionnaire about perceived skin condition and product satisfaction at baseline, week 4, and week 8.
- Have facial photographs taken for skin condition evaluation, with identifiable areas masked before disclosure.
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 Oct 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
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2026
CompletedFirst Submitted
Initial submission to the registry
July 9, 2026
CompletedFirst Posted
Study publicly available on registry
July 23, 2026
CompletedJuly 23, 2026
July 1, 2026
4 months
July 9, 2026
July 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Facial Skin Analysis Parameters
VISIA Micro-Analysis Skin Image Analyzer was utilized to measure skin spots, wrinkles, texture, pores, UV spots, brown Spots, red areas, porphyrins. Units: arbitrary units. Facial skin condition will be assessed using non-invasive image-based facial skin analysis. Changes from baseline will be evaluated at week 4 and week 8.
Baseline, week 4, and week 8
Skin Moisture
Skin moisture meter (VapoMeter) was utilized to measure skin moisture. Units: g/m²h Facial skin condition will be assessed using non-invasive image-based facial skin analysis. Changes from baseline will be evaluated at week 4 and week 8.
Baseline, week 4, and week 8
Skin elasticity
Skin elastometer (Soft Plus) was utilized to measure skin elasticity. Units: arbitrary units. Facial skin condition will be assessed using non-invasive image-based facial skin analysis. Changes from baseline will be evaluated at week 4 and week 8.
Baseline, week 4, and week 8
Study Arms (2)
BeauSaki Edible Bird's Nest Peptide Group
EXPERIMENTALParticipants in this group will take one capsule of BeauSaki Edible Bird's Nest Peptide Product daily for 8 weeks.
Placebo Group
PLACEBO COMPARATORParticipants in this group will take one placebo capsule without edible bird's nest daily for 8 weeks.
Interventions
Participants will take one capsule daily for 8 weeks.
Participants will take one placebo capsule without edible bird's nest daily for 8 weeks.
Eligibility Criteria
You may qualify if:
- Participants aged over 18 years.
You may not qualify if:
- Individuals who are unwilling to participate voluntarily.
- Individuals diagnosed by a physician with skin disease, liver cirrhosis, or chronic renal failure.
- Individuals with known allergies to cosmetics, drugs, or foods.
- Pregnant or breastfeeding individuals.
- Individuals taking medications for chronic diseases.
- Students taught by the principal investigator.
- Individuals unwilling to allow their study-related photographs to be disclosed. Vegetarians.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Chia Nan University of Pharmacy & Science
Tainan, Taiwan, 71710, Taiwan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 9, 2026
First Posted
July 23, 2026
Study Start
October 1, 2025
Primary Completion
January 31, 2026
Study Completion
March 31, 2026
Last Updated
July 23, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share