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A Clinical Trial to Evaluate the Effects of a Skin Balm on the Appearance of the Eye Area

A Clinical Trial to Evaluate the Effects of a Skin Balm on the Appearance of the Eye Area

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06452810
Enrollment
35
Registered
2024-06-11
Start date
2024-02-29
Completion date
2024-05-03
Last updated
2024-06-11

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

Conditions

Skin Health

Keywords

Eye Balm, Periorbital area, Dermatology

Brief summary

This virtual single-group clinical trial aims to evaluate the effects of the Sahajan Golden Glow Balm on the health and appearance of the skin in the periorbital area over a period of 6 weeks. Participants will apply the product twice daily and complete questionnaires at various intervals. Photos for expert skin grading will be taken at Baseline and Week 6.

Detailed description

The study will investigate the impact of Sahajan Golden Glow Balm on skin health, particularly focusing on fine lines, wrinkles, dark circles, and dry eyes. It involves 35 female participants aged 35 and above, who will use the product for 6 weeks and complete periodic questionnaires and provide photos for dermatological assessment.

Interventions

DIETARY_SUPPLEMENTExperimental: Sahajan Golden Glow Balm

Participants will apply the Sahajan Golden Glow Balm twice daily (morning and night) to the periorbital area following the specified instructions.

Sponsors

Citruslabs
CollaboratorINDUSTRY
Sahajan
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Masking description

Masking: None (Open Label)

Intervention model description

Study Type: Interventional (Clinical Trial) Estimated Enrollment: 35 participants Allocation: Non-randomized Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment

Eligibility

Sex/Gender
FEMALE
Age
35 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Concerns with the appearance of skin in the periorbital area * Willing to maintain the same skincare routine for the study duration * Must own a smartphone or digital camera for photos

Exclusion criteria

* Medical conditions affecting skin health * Use of medications or products that could affect skin health * Pregnancy or breastfeeding * Participation in another clinical study

Design outcomes

Primary

MeasureTime frameDescription
Changes in the Health and Appearance of the Skin in the Periorbital AreaBaseline to Week 6The primary outcome measure will assess changes in the health and appearance of the skin in the periorbital area, evaluated via expert skin grading by a board-certified dermatologist.

Secondary

MeasureTime frameDescription
Changes in Participants' Perception of the Appearance of the Skin in the Periorbital AreaBaseline, Day 1, Week 2, Week 4, and Week 6The secondary outcome measure will evaluate changes in participants' perception of the appearance of their skin in the periorbital area, including the appearance of fine lines, wrinkles, dark circles, and dry skin, using participant-reported questionnaires.

Countries

United States

Outcome results

None listed

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