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A Clinical Trial to Evaluate the Effects of an Eye Serum on Improving the Appearance of the Periorbital Area

A Clinical Trial to Evaluate the Effects of an Eye Serum on Improving the Appearance of the Periorbital Area

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06143033
Enrollment
35
Registered
2023-11-22
Start date
2023-08-21
Completion date
2024-02-15
Last updated
2024-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periorbital Area

Brief summary

This study will evaluate the efficacy of the DIME Beauty Luminosity Eye Serum in improving the appearance of skin in the periorbital eye area. This study will last for 60 days. The study will be conducted as a single-arm trial in which all participants will use the test products. Participants will be required to complete questionnaires at Baseline, Day 30, and Day 60, photos will be taken at Baseline, Day 30, and Day 60, and expert skin grading will take place at Baseline and Day 60.

Interventions

OTHERDIME Beauty Luminosity Eye Serum

Test product contains: Water/Aqua, Organic Aloe Vera Juice, Lycium Barbarum (Goji Berry) Fruit Extract, Vitis Vinifera (Grape Seed) Extract, Cucumis Sativus (Cucumber) Extract, Glycerin, Niacinamide, Squalane, Camellia Seed Oil, DL-Panthenol (Vitamin B5), Carbomer, Sodium Hyaluronate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Phenoxyethenol, Caprylyl Glycol, Acacia Senegal Gum, Caffeine, Helianthus Annuus (Sunflower) Seed Oil, Malus Domestica (Apple) Fruit Stem Cell Extract, Argania Spinosa (Argan) Sprout Stem Cell Extract, Tetrahexyldecyl Ascorbate (Vitamin C), Acetyl Tetrapeptide, Acetyl Hexapeptide-8, Vitamin E Mixed Tocopherols, Sodium Hydroxide.

Sponsors

Citruslabs
CollaboratorINDUSTRY
Dime Beauty Co.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Females age 18-65. * Have visible dark circles under the eyes. * Have puffy eyes. * Have bags under the eyes. * Have visible fine lines and wrinkles around the eyes. * Have a smartphone or camera to take before-and-after selfies.

Exclusion criteria

* Anyone not in good health. * Anyone who has any chronic health conditions such as oncological or psychiatric disorders. * Anyone who has any known serious allergic reactions that require the use of an Epi-Pen. * Anyone who is pregnant, breastfeeding, or wanting to become pregnant over the next three months. * Anyone who cannot/ will not commit to the study protocol. * Anyone with a history of substance abuse.

Design outcomes

Primary

MeasureTime frameDescription
Change in appearance of periorbital puffiness. [Baseline to Day 60]60 daysMeasured via expert skin grading of before & after photos conducted by a board-certified dermatologist.
Change in appearance of dark circles underneath eyes. [Baseline to Day 60]60 daysMeasured via expert skin grading of before & after photos conducted by a board-certified dermatologist.
Change in participants' perception of the appearance of periorbital puffiness. [Baseline to Day 60]60 daysMeasured via study-specific surveys. Surveys will be completed by participants and are designed using a 5-point Likert scale, with th 5 representing the most favorable/best outcome (e.g., Not at all) and 1 representing the least favorable/worst outcome (e.g., Severe).
Change in participants' perception of the appearance of dark circles underneath eyes. [Baseline to Day 60]60 daysMeasured via study-specific surveys. Surveys will be completed by participants and are designed using a 5-point Likert scale, with th 5 representing the most favorable/best outcome (e.g., Not at all) and 1 representing the least favorable/worst outcome (e.g., Severe).

Secondary

MeasureTime frameDescription
Change in appearance of fine lines and wrinkles in the eye area. [Baseline to Day 60]60 daysMeasured via expert skin grading of before & after photos conducted by a board-certified dermatologist.
Change in participants' perception of the appearance of fine lines and wrinkles in the eye area. [Baseline to Day 60]60 daysMeasured via study-specific surveys. Surveys will be completed by participants and are designed using a 5-point Likert scale, with th 5 representing the most favorable/best outcome (e.g., Not at all) and 1 representing the least favorable/worst outcome (e.g., Severe).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026