Improved Skin Anti-aging Outcomes Associated With Collagen Fortified Consumption In 30 to 50-Year-old Women
Skin Laxity, Skin Lines
About this trial
This is an interventional supportive care trial for Skin Laxity focused on measuring Collagen, skin anti-aging, skin moisture, skin elasticity
Eligibility Criteria
Inclusion Criteria: Chinese females, age between 30-50; Be in general good health; Understand the test procedure, read, and sign an appropriate Informed Consent Form indicating their willingness to participate; Have mild to moderate darker skin tone 3 on Unilever visual scale of 1~9; Have mild pigmentation level 2 on Unilever visual scale of 0~9; Have visual grading score on crow's feet 3 on Unilever visual scale of 0~9; Have visual grading score on peri-oral 3 on Unilever visual scale of 0~9; Have visual grading score on nasolabial folds 3 on Unilever visual scale of 0~9; Tolerate to well-known anti-aging actives; Agree to not use any other creams, lotions, moisturizers on the face, other than what is provided for the duration of the study; Agree to refrain from wearing make-up (such as foundation, eye shadow, lipstick etc.) or any skin care products on the face on the study visits; Agree to avoid washing the treatment site area for two hours following product application and agree to avoid washing appliances (i.e., sponge, wash cloth, loofah, etc.). Exclusion Criteria: Have used any skin lightening /anti-aging benefits products at least one month before this study Subject having done facial injections and/or aesthetic surgery. Be involved in any aspect of test administration, i.e., evaluating or overseeing activities related to product. Have participated in any clinical study involving the test sites within the previous 6 months, or is subject participating in any clinical study concurrently. Have a history of any type of bagcer, including but not limited to any type of skin bagcer (squamous or basal cell carcinoma at the treatment site) or history of malignant melanoma at any body site. Have a history of skin disease or the presence of a skin condition on the test sites that the Investigator feels would interfere with the study. Be taking antihistamines (> 3x/week) or anti-inflammatory (> 8x/week) on a regular basis, or has the subject taken systemic or topical steroidal medications within 4 weeks of study enrolment. Have any of the following conditions or factors that the investigator believes may affect the response of the skin or the interpretation of the test results, including, but not limited to, diabetes, pregnancy, lactation. Have any cuts/abrasions on the test site at baseline. Have had a suspicious skin lesion removed by a dermatologist at any time. The subject is an employee of sponsor or the site conducting the study.
Sites / Locations
- Ai'er Hospital
- SPRIM Central Lab
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Study product plus collagen supplement
Study product without collagen supplement
5g/bag, containing the following ingredients per 5g serving: Collagen tripeptide 1500 mg Elastin peptide 150 mg
5g/bag, containing the following ingredients per 5g serving: Peach juice 8 mg Erythritol 10 mg