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A Single-Group Study to Evaluate the Effects of an Eyelash Serum on Improving Eyelash Growth

A Single-Group Study to Evaluate the Effects of an Eyelash Serum on Improving Eyelash Growth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06125730
Enrollment
35
Registered
2023-11-09
Start date
2023-08-23
Completion date
2024-02-10
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

Eyelash Growth

Brief summary

This study will evaluate the efficacy of the DIME Beauty Eyelash Boost Serum in improving the growth of the eyelashes and their appearance in terms of length, fullness, and thickness. 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 product. Participants will be required to undertake questionnaires at Baseline, Day 30, and Day 60, photos will be taken at Baseline, Day 30, and Day 60, and expert eyelash grading will take place at Baseline and Day 60.

Interventions

OTHERDIME Beauty Eyelash Boost Serum

The test product contains Water, Glycerin, Amino Acids (Sodium PCA, Sodium Lactate, Arginine, Aspartic Acid, PCA, Glycine, Alanine, Serine, Valine, Proline, Threonine, Isoleucine, Histidine, Phenylalanine), Hyaluronic Acid, Panthenol, Aloe Leaf Extract, Niacinamide, Purslane, Chebulic Fruit Extract, Apple Fruit Extract, Tocopherol, Phenoxyethanol, Hexanediol, Ethylhexylglycerin, Biotinoyl Tripeptide-1, Myristoyl Pentapeptide-4.

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 aged 18-65. Wish to improve their eyelash growth. Wish to improve their eyelash length, thickness, and fullness. 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 undergone any procedures that target the eyelashes in the past 3 months, or is planning to in the next 60 days. This includes eyelash lifts, tints, and extensions. Anyone who has recently started using any product or taking any supplements that target eyelash growth, or who is planning to in the next 60 days. 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
Changes in eyelash growth as per expert grading. [Timeframe: Baseline to Day 60]60 daysBefore & after photos of the eyelashes will undergo grading by an eyelash expert.
Changes in participant-perceived eyelash growth. [Timeframe: Baseline to Day 60]60 daysMeasured via study-specific surveys. Surveys will be adapted from the validated Eyelash Satisfaction Questionnaire and designed on a 5-point Likert scale, with 5 representing the most favorable/best outcome (e.g., Excellent) and 1 representing the least favorable/worst outcome (e.g., Very poor).

Countries

United States

Outcome results

None listed

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