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Efficacy Testing of Collagen Peptide Drink

Efficacy Testing of Collagen Peptide Drink

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04996043
Enrollment
60
Registered
2021-08-09
Start date
2021-05-17
Completion date
2021-11-25
Last updated
2022-01-05

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 Collagen Peptide Drink on skin condition improvement

Interventions

DIETARY_SUPPLEMENTCollagen Peptide Drink

Testing product

DIETARY_SUPPLEMENTPlacebo drink

Blank

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 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. * Constant drug use * Participated cosmetic product human study in the past 3 months.

Design outcomes

Primary

MeasureTime frameDescription
The change of skin wrinklesChange from Baseline skin wrinkles at 4 weeksVISIA Complexion Analysis System was utilized to measure skin wrinkles. Units: arbitrary units
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 collagen densityChange from Baseline skin collagen density at 4 weeksDermaLab® Series SkinLab Combo was utilized to measure skin pores. Units: arbitrary units
The change of skin elasticityChange from Baseline skin elasticity at 4 weeksSoft Plus was utilized to measure skin elasticity. Units: arbitrary units
The change of MMP-1 of bloodChange from Baseline MMP-1 at 4 weeksVenous blood was sampled to measure MMP-1
The change of TIMP-1 of bloodChange from Baseline TIMP-1 at 4 weeksVenous blood was sampled to measure TIMP-1

Secondary

MeasureTime frameDescription
The change of blood total antioxidant capacity (TAC)Change from Baseline TAC at 4 weeksVenous blood was sampled to measure concentrations of TAC
The change of IL-10 of bloodChange from Baseline IL-10 at 4 weeksVenous blood was sampled to measure IL-10
The change of SOD-RBC of bloodChange from Baseline SOD-RBC at 4 weeksVenous blood was sampled to measure SOD-RBC
The change of f-thiols of bloodChange from Baseline f-thiols at 4 weeksVenous blood was sampled to measure f-thiols
The change of t-GSH of bloodChange from Baseline t-GSH at 4 weeksVenous blood was sampled to measure t-GSH
The change of GST-RBC of bloodChange from Baseline GST-RBC at 4 weeksVenous blood was sampled to measure GST-RBC
The change of MDA of bloodChange from Baseline MDA at 4 weeksVenous blood was sampled to measure MDA
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 melanin indexChange from Baseline skin melanin index at 4 weeksSoft Plus was utilized to measure skin melanin index. Units: arbitrary units
The change of skin L* valueChange from Baseline L* value at 4 weeksChroma Meter MM500 was utilized to measure skin L\* value. Units: arbitrary units, 0-100
The change of skin spotsChange from Baseline skin spots at 4 weeksVISIA Complexion Analysis System was utilized to measure skin spots. Units: arbitrary units
The change of skin UV spotsChange from Baseline skin UV spots at 4 weeksVISIA Complexion Analysis System was utilized to measure skin UV spots. Units: arbitrary units
The change of skin brown spotsChange from Baseline skin brown spots at 4 weeksVISIA Complexion Analysis System was utilized to measure skin brown spots. Units: arbitrary units
The change of TNF-α of bloodChange from Baseline TNF-α at 4 weeksVenous blood was sampled to measure TNF-α

Other

MeasureTime frameDescription
The change of SGPT of bloodChange from Baseline SGPT at 4 weeksVenous blood was sampled to measure SGPT
The change of BUN of bloodChange from Baseline BUN at 4 weeksVenous blood was sampled to measure BUN
The change of creatinine of bloodChange from Baseline creatinine at 4 weeksVenous blood was sampled to measure creatinine
The change of uric acid of bloodChange from Baseline uric acid at 4 weeksVenous blood was sampled to measure uric acid
The change of triglyceride of bloodChange from Baseline triglyceride at 4 weeksVenous blood was sampled to measure triglyceride
The change of total cholesterol of bloodChange from Baseline total cholesterol at 4 weeksVenous blood was sampled to measure total cholesterol
The change of SGOT of bloodChange from Baseline SGOT at 4 weeksVenous blood was sampled to measure SGOT

Countries

Taiwan

Outcome results

None listed

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