Facial SPF Study

Study Number: C25-D107

Study Location:

Dallas Research Center: 1801 N. Glenville Dr., Suite 250 Richardson, Texas 75081

Compensation: Up to $400.00

Gender:

Male and Female

Age:

18-55 years old

Skin Type:

Fitz I-VI

Study Description:

This single-center cosmetic clinical trial aims to evaluate the efficacy and tolerability of the Sponsor's facial product over an 8-week period. The study will include male and female participants exhibiting mild to moderate tactile roughness on the cheeks, as well as visual signs of skin aging and unevenness across the entire face. These include fine lines, visual roughness, uneven skin tone, hyperpigmentation (dark spots), redness, diminished radiance/luminosity.

Study Requirements:

Must:

✓ Bring your regularly used basic (without antiaging claims or ingredients) facial skin care products (cleansers/soaps, moisturizers, toners, and/or serums) and sunscreen (at least SPF 30) with a history of safe usage to your first visit for documentation.
✓ Fine lines, visual roughness, uneven skin tone, hyperpigmentation (dark spots), redness, diminished radiance/luminosity.

Cannot:

✕ Cannot have any autoimmune disorders, connective tissue diseases, or immune deficiencies (such as lupus, Crohn’s disease, HIV, or rheumatoid arthritis).

Complete the prescreening survey below:

All information you provide will be kept confidential; you may be contacted by telephone or text. The questions in the survey will be used to determine your eligibility for our studies. If you withdraw or do not qualify, your information will be stored for future reference. You can request to have your information disabled at any time, and we will not contact you for future studies.

Screening Survey

CCPA

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