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Efficacy Evaluation of Triple up® Collagen Drink on Skin Condition

Efficacy Evaluation of Triple up® Collagen Drink on Skin Condition

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04225091
Enrollment
50
Registered
2020-01-13
Start date
2020-01-30
Completion date
2020-05-07
Last updated
2020-11-30

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

Conditions

Skin Condition

Brief summary

To assess Triple up® Collagen Drink on skin condition improvement

Interventions

DIETARY_SUPPLEMENTTesting product

consume 1 bottle (50 mL) per day for 28 days

DIETARY_SUPPLEMENTBlank

consume 1 bottle (50 mL) per day for 28 days

Sponsors

TCI Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

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, heart, liver, kidney, endocrine and other organs and patients with mental illness (according to medical history). * 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 in the past 4 weeks. * Vegetarian * Subjects who have large spots (area \>3 square centimeter) or abnormal acne.

Design outcomes

Primary

MeasureTime frameDescription
The change of skin moistureChange from Baseline skin moisture at 4 weeksCorneometer® CM825 was utilized to measure skin moisture. Units: arbitrary Corneometer® units 0-120
The change of skin elasticityChange from Baseline skin elasticity at 4 weeksCutometer® dual MPA 580 was utilized to measure skin elasticity (parameter R2). Units: μm penetration depth into the probe opening, expressed as curves
The change of skin wrinklesChange from Baseline skin wrinkles at 4 weeksVISIA Complexion Analysis System was utilized to measure wrinkles. Units: arbitrary units
The change of skin collagen densityChange from Baseline skin collagen density at 4 weeksDermaLab® USB - 20 MHz High Freq. Ultrasound probe was utilized to scan and analyze skin collagen density. Units: Intensity score

Secondary

MeasureTime frameDescription
The change of skin textureChange from Baseline skin texture at 4 weeksVISIA Complexion Analysis System was utilized to measure skin texture. Units: arbitrary units
The change of skin poresChange from Baseline skin pores at 4 weeksVISIA Complexion Analysis System was utilized to measure skin pores. Units: arbitrary units

Countries

Taiwan

Outcome results

None listed

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