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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06452810
Other study ID # 20407
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 29, 2024
Est. completion date May 3, 2024

Study information

Verified date June 2024
Source Sahajan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date May 3, 2024
Est. primary completion date May 3, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 35 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Experimental: 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.

Locations

Country Name City State
United States Citruslabs Santa Monica California

Sponsors (2)

Lead Sponsor Collaborator
Sahajan Citruslabs

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in the Health and Appearance of the Skin in the Periorbital Area The 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. Baseline to Week 6
Secondary Changes in Participants' Perception of the Appearance of the Skin in the Periorbital Area The 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. Baseline, Day 1, Week 2, Week 4, and Week 6
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