NCT06125730

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 23, 2023

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

November 4, 2023

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 9, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 10, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 10, 2024

Completed
Last Updated

February 22, 2024

Status Verified

February 1, 2024

Enrollment Period

6 months

First QC Date

November 4, 2023

Last Update Submit

February 20, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • Changes in eyelash growth as per expert grading. [Timeframe: Baseline to Day 60]

    Before \& after photos of the eyelashes will undergo grading by an eyelash expert.

    60 days

  • Changes in participant-perceived eyelash growth. [Timeframe: Baseline to Day 60]

    Measured 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").

    60 days

Study Arms (1)

DIME Beauty Eyelash Boost Serum

EXPERIMENTAL

Participants will use the eyelash serum twice daily in the morning and evening. The serum will be applied to the base of the top and bottom lashes.

Other: DIME Beauty Eyelash Boost Serum

Interventions

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.

DIME Beauty Eyelash Boost Serum

Eligibility Criteria

Age18 Years - 65 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Citruslabs

Santa Monica, California, 90404, United States

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 4, 2023

First Posted

November 9, 2023

Study Start

August 23, 2023

Primary Completion

February 10, 2024

Study Completion

February 10, 2024

Last Updated

February 22, 2024

Record last verified: 2024-02

Locations