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Safety and Efficacy of a Hydrolyzed Collagen Formulation (HYCOS) for Facial Skin Elasticity and Wrinkles: A Randomized, Double-Blind, Placebo-Controlled Trial
Journal of Cosmetic Dermatology
2026
25(9):e71121
Bibliography
- Trial registry
- View on ClinicalTrials.gov Registered trial — results not yet published in a peer-reviewed journal.
- Funding
- Funded by Blackmores Institute, Australia, which supplied HYCOS and placebo and supported trial conduct; additional support came from Naresuan University research funds and PERCH-CIC. The paper states the sponsor had no role in data analysis, interpretation, or the publication decision.
- Competing interests
- The authors declared no conflicts of interest.
Study snapshot
| Design | 12-week randomized, double-blind, placebo-controlled clinical trial |
|---|---|
| Model | Healthy Thai adults aged 30–60 years with mild-to-moderate facial crow's-feet wrinkles |
| Sample | 140 randomized; 135 completed (66 active, 69 placebo) |
| Intervention | One HYCOS sachet daily containing hydrolyzed collagen peptides 5,000 mg, glutathione 250 mg, and vitamin E (D-alpha-tocopherol succinate) 11.5 mg, plus excipients, versus matched placebo. |
| Duration | 12 weeks |
| Endpoints | Skin hydration by Corneometer; Skin elasticity by Cutometer (R2, R5, R7); Crow's-feet wrinkle roughness by PRIMOS 3D imaging; Dermatologist wrinkle grading; Participant self-assessment; Adverse events and laboratory safety |
What the study showed, in plain terms
Key findings
What this study can and cannot tell us
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