Efficacy Evaluation of Triple up® Collagen Drink on Skin Condition

Skin Condition Clinical Trial

Official title:

Efficacy Evaluation of Triple up® Collagen Drink on Skin Condition

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04225091
• Other study ID #: 19-098-B
• Status: Completed
• Phase: N/A
• Start date: January 30, 2020
• Est. completion date: May 7, 2020

Study information

• Verified date: November 2020
• Source: TCI Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To assess Triple up® Collagen Drink on skin condition improvement

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: May 7, 2020
• Est. primary completion date: April 21, 2020
• 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, 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.

Related Conditions & MeSH terms

• Disease
• Skin Condition
• Skin Diseases

Intervention

Dietary Supplement:
• Testing product
consume 1 bottle (50 mL) per day for 28 days
• Blank
consume 1 bottle (50 mL) per day for 28 days

Locations

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

Sponsors (1)

Lead Sponsor	Collaborator
TCI Co., Ltd.

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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 4 weeks
Primary	The change of skin elasticity	Cutometer® dual MPA 580 was utilized to measure skin elasticity (parameter R2). Units: µm penetration depth into the probe opening, expressed as curves	Change from Baseline skin elasticity at 4 weeks
Primary	The change of skin wrinkles	VISIA Complexion Analysis System was utilized to measure wrinkles. Units: arbitrary units	Change from Baseline skin wrinkles at 4 weeks
Primary	The change of skin collagen density	DermaLab® USB - 20 MHz High Freq. Ultrasound probe was utilized to scan and analyze skin collagen density. Units: Intensity score	Change from Baseline skin collagen density at 4 weeks
Secondary	The change of skin texture	VISIA Complexion Analysis System was utilized to measure skin texture. Units: arbitrary units	Change from Baseline skin texture at 4 weeks
Secondary	The change of skin pores	VISIA Complexion Analysis System was utilized to measure skin pores. Units: arbitrary units	Change from Baseline skin pores at 4 weeks