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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05376657
Other study ID # 22-010-B
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2022
Est. completion date September 3, 2022

Study information

Verified date September 2022
Source TCI Co., Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess cherry collagen drink on skin condition improvement


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date September 3, 2022
Est. primary completion date July 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years and older
Eligibility 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


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Cherry collagen drink
consume 1 sachet per day
Placebo drink
consume 1 sachet per day

Locations

Country Name City State
Taiwan Chia Nan University of Pharmacy & Science Tainan City

Sponsors (1)

Lead Sponsor Collaborator
TCI Co., Ltd.

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Other The change of liver function biomarkers (AST, ALT) of blood Venous blood was sampled to measure liver function biomarkers Change from Baseline liver function biomarkers at 8 weeks
Other The change of renal function biomarkers (creatinine, BUN) of blood Venous blood was sampled to measure renal function biomarkers Change from Baseline renal function biomarkers at 8 weeks
Other The change of self-assessment skin condition A self-assessment questionnaire was collected to evaluate skin condition Change from Baseline skin condition at 8 weeks
Primary The change of skin wrinkles VISIA Complexion Analysis System was utilized to measure skin wrinkles. Units: arbitrary units Change from Baseline skin wrinkles at 8 weeks
Primary The change of skin texture VISIA Complexion Analysis System was utilized to measure skin texture. Units: arbitrary units Change from Baseline skin texture at 8 weeks
Primary The change of skin collagen density DermaLab® Series SkinLab Combo was utilized to measure skin pores. Units: arbitrary units Change from Baseline skin collagen density at 8 weeks
Primary The change of skin elasticity Soft Plus was utilized to measure skin elasticity. Units: arbitrary units Change from Baseline skin elasticity at 8 weeks
Secondary The change of skin melanin index Soft Plus was utilized to measure skin melanin index. Units: arbitrary units Change from Baseline skin melanin index at 8 weeks
Secondary The change of skin L* value Chroma Meter MM500 was utilized to measure skin L* value. Units: arbitrary units, 0-100 Change from Baseline L* value at 8 weeks
Secondary The change of skin moisture Corneometer® CM825 was utilized to measure skin moisture. Units: arbitrary Corneometer® units 0-120 Change from Baseline skin moisture at 8 weeks
Secondary The change of skin spots VISIA Complexion Analysis System was utilized to measure skin spots. Units: arbitrary units Change from Baseline skin spots at 8 weeks
Secondary The change of skin UV spots VISIA Complexion Analysis System was utilized to measure skin UV spots. Units: arbitrary units Change from Baseline skin UV spots at 8 weeks
Secondary The change of skin brown spots VISIA Complexion Analysis System was utilized to measure skin brown spots. Units: arbitrary units Change from Baseline skin brown spots at 8 weeks
Secondary The change of SOD-RBC of blood Venous blood was sampled to measure SOD-RBC Change from Baseline SOD-RBC at 8 weeks
Secondary The change of t-GSH of blood Venous blood was sampled to measure t-GSH Change from Baseline t-GSH at 8 weeks
Secondary The change of GST-RBC of blood Venous blood was sampled to measure GST-RBC Change from Baseline GST-RBC at 8 weeks
Secondary The change of blood total antioxidant capacity (TAC) Venous blood was sampled to measure concentrations of TAC Change from Baseline TAC at 8 weeks
Secondary The change of desmosine of blood Venous blood was sampled to measure concentrations of desmosine Change from Baseline desmosine at 8 weeks
Secondary The change of TNF-alpha of blood Venous blood was sampled to measure concentrations of TNF-alpha Change from Baseline TNF-alpha at 8 weeks
Secondary The change of transepidermal water loss (TEWL) Tewameter® TM300 was utilized to measure TEWL. Units: g/hm² Change from Baseline TEWL at 8 weeks
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