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Efficacy Testing of Collagen Drink on Skin Beauty and Sleep Aid

Efficacy Testing of Collagen Drink on Skin Beauty and Sleep Aid

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05182814
Enrollment
60
Registered
2022-01-10
Start date
2021-11-10
Completion date
2022-04-30
Last updated
2022-06-13

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

Conditions

Skin Condition, Sleep Disturbance

Brief summary

To assess Collagen Drink on skin condition and sleep quality improvement

Interventions

DIETARY_SUPPLEMENTPlacebo drink

Blank

DIETARY_SUPPLEMENTCollagen Juice Drink

Testing product

Sponsors

TCI Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

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 * Constant drug use * Received facial laser therapy, chemical peeling or UV overexposure (\>3 hours everyday) in the past 4 weeks. * Students taught by the PI

Design outcomes

Primary

MeasureTime frameDescription
The change of desmosine of bloodChange from Baseline desmosine at 8 weeksVenous blood was sampled to measure desmosine
The change of skin wrinklesChange from Baseline skin wrinkles at 8 weeksVISIA Complexion Analysis System was utilized to measure skin wrinkles. Units: arbitrary units
The change of skin textureChange from Baseline skin texture at 8 weeksVISIA 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 weeksDermaLab® Series SkinLab Combo was utilized to measure skin pores. Units: arbitrary units
The change of skin elasticityChange from Baseline skin elasticity at 8 weeksCutometer® MPA580 was utilized to measure skin elasticity. Units: arbitrary units
The change of skin L* valueChange from Baseline L* value at 8 weeksChroma Meter MM500 was utilized to measure skin L\* value. Units: arbitrary units, 0-100
The change of TIMP-1 of bloodChange from Baseline TIMP-1 at 8 weeksVenous blood was sampled to measure TIMP-1
The change of sleep qualityChange from Baseline sleep quality at 8 weeksSelf-assessment questionnaire was utilized to survey sleep quality.
The change of AGEs of bloodChange from Baseline AGEs at 8 weeksVenous blood was sampled to measure AGEs

Secondary

MeasureTime frameDescription
The change of skin poresChange from Baseline skin pores at 8 weeksVISIA Complexion Analysis System was utilized to measure skin pores. Units: arbitrary units
The change of skin a* valueChange from Baseline skin a* value at 8 weeksChroma Meter MM500 was utilized to measure skin a\* value. Units: arbitrary units
The change of skin hydrationChange from Baseline skin hydration at 8 weeksCorneometer® CM825 was utilized to measure skin hydration. Units: arbitrary Corneometer® units 0-120
The change of transepidermal water lossChange from Baseline transepidermal water loss at 8 weeksTewameter® TM300 was utilized to measure skin hydration. Units: g/hm²
The change of skin melanin indexChange from Baseline skin melanin index at 8 weeksSoft Plus was utilized to measure skin melanin index. Units: arbitrary units

Countries

Taiwan

Outcome results

None listed

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