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Evaluation of Antioxidant and Skin Beauty Effects of Cherry Collagen Drink

Not Applicable
Completed
Conditions
Skin Condition
Registration Number
NCT05376657
Lead Sponsor
TCI Co., Ltd.
Brief Summary

To assess cherry collagen drink on skin condition improvement

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Healthy adults aged above 20 years old
Exclusion Criteria
  • Subject who is not willing to participate in this study.
  • Patients with diseases of the skin, liver, kidney.
  • Subjects who have known cosmetic, drug or food allergies, difficulty in digestive tract absorption or disorder.
  • Female who is pregnant or nursing or planning to become pregnant during the course of the study.
  • Received facial laser therapy, chemical peeling or UV overexposure (> 3 hr/week) in the past 4 weeks.
  • Constant drug use
  • Students who are currently taking courses taught by the principal investigator of this trial.
  • Body weight < 50 kg.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
The change of skin wrinklesChange from Baseline skin wrinkles at 8 weeks

VISIA Complexion Analysis System was utilized to measure skin wrinkles. Units: arbitrary units

The change of skin textureChange from Baseline skin texture at 8 weeks

VISIA Complexion Analysis System was utilized to measure skin texture. Units: arbitrary units

The change of skin collagen densityChange from Baseline skin collagen density at 8 weeks

DermaLab® Series SkinLab Combo was utilized to measure skin pores. Units: arbitrary units

The change of skin elasticityChange from Baseline skin elasticity at 8 weeks

Soft Plus was utilized to measure skin elasticity. Units: arbitrary units

Secondary Outcome Measures
NameTimeMethod
The change of skin melanin indexChange from Baseline skin melanin index at 8 weeks

Soft Plus was utilized to measure skin melanin index. Units: arbitrary units

The change of skin moistureChange from Baseline skin moisture at 8 weeks

Corneometer® CM825 was utilized to measure skin moisture. Units: arbitrary Corneometer® units 0-120

The change of skin spotsChange from Baseline skin spots at 8 weeks

VISIA Complexion Analysis System was utilized to measure skin spots. Units: arbitrary units

The change of skin brown spotsChange from Baseline skin brown spots at 8 weeks

VISIA Complexion Analysis System was utilized to measure skin brown spots. Units: arbitrary units

The change of SOD-RBC of bloodChange from Baseline SOD-RBC at 8 weeks

Venous blood was sampled to measure SOD-RBC

The change of desmosine of bloodChange from Baseline desmosine at 8 weeks

Venous blood was sampled to measure concentrations of desmosine

The change of TNF-alpha of bloodChange from Baseline TNF-alpha at 8 weeks

Venous blood was sampled to measure concentrations of TNF-alpha

The change of transepidermal water loss (TEWL)Change from Baseline TEWL at 8 weeks

Tewameter® TM300 was utilized to measure TEWL. Units: g/hm²

The change of skin UV spotsChange from Baseline skin UV spots at 8 weeks

VISIA Complexion Analysis System was utilized to measure skin UV spots. Units: arbitrary units

The change of t-GSH of bloodChange from Baseline t-GSH at 8 weeks

Venous blood was sampled to measure t-GSH

The change of GST-RBC of bloodChange from Baseline GST-RBC at 8 weeks

Venous blood was sampled to measure GST-RBC

The change of skin L* valueChange from Baseline L* value at 8 weeks

Chroma Meter MM500 was utilized to measure skin L\* value. Units: arbitrary units, 0-100

The change of blood total antioxidant capacity (TAC)Change from Baseline TAC at 8 weeks

Venous blood was sampled to measure concentrations of TAC

Trial Locations

Locations (1)

Chia Nan University of Pharmacy & Science

🇨🇳

Tainan City, Taiwan

Chia Nan University of Pharmacy & Science
🇨🇳Tainan City, Taiwan

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