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Completed NCT07900308

A Clinical Study to Assess the Effectiveness of the Hyper Glow Serum on Skin Complexion and Hydration

Conditions: Poor Facial Skin Complexion, Skin Hydration, Skin Texture, Skin Evenness, Skin Tightness

Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 35
Sponsor: Dime Beauty Co.

Location: Citruslabs Las Vegas Nevada

Summary

This single-group, open-label, virtual clinical trial will evaluate the effectiveness of the Hyper Glow Serum by DIME Beauty on skin complexion and hydration in 35 female participants over 60 days. Participants will apply 3-5 drops of the serum to the face and neck each morning, with assessments conducted via self-reported questionnaires, expert skin grading, and before-and-after photographs at Baseline, Day 14, Day 30, and Day 60. The primary objective is to examine the effect of daily use of the Hyper Glow Serum on overall skin complexion, including texture, evenness, and brightness. The secondary objective is to assess changes in participants' perception of skin hydration, tightness, and youthfulness over the 60-day intervention period.

Eligibility Criteria

Inclusion Criteria: * Female * Individuals aged 18-65 * Individuals with no known allergies to the product ingredients * Individuals willing to comply with the study requirements * Self-reported poor facial skin complexion * Self-reported issues with skin hydration and tightness * Generally healthy - do not live with any uncontrolled chronic disease * Must not use any other oil-based serums for the duration of the study * Willing to maintain the same skincare products and routine for the duration of the study (apart from other serums) * Has been using the same skincare products and routine for the past month Exclusion Criteria: * Individuals with known skin conditions or diseases of the face and neck * Individuals currently on medication that affects skin health * Individuals who have undergone facial cosmetic procedures in the past six months * Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders * Women who are pregnant, breastfeeding, or trying to conceive * Anyone unwilling to follow the study protocol * Anyone currently participating or planning to participate in a research study

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07900308). StuddyBuddy aggregates publicly available trial information.