Status:
UNKNOWN
Effects of an Oral Herbal Supplement on Skin Aging, Hydration, and Elasticity
Lead Sponsor:
Integrative Skin Science and Research
Collaborating Sponsors:
Vidya Herbs
Conditions:
Photoaging
Eligibility:
FEMALE
35-55 years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate how an oral herbal supplementation influences facial skin elasticity and facial hydration as well as markers of photoaging (erythema and pigmentation).
Detailed Description
Skin is the largest organ of the body and skin aging represents a primary indicator of the aging process in the body. Photoaging is among the most crucial factors that cause skin aging damage. Photoag...
Eligibility Criteria
Inclusion
- \- Women who are 35 to 55 years of age
Exclusion
- Individuals who are pregnant or breastfeeding.
- Prisoners.
- Adults unable to consent.
- Those who are unwilling to discontinue topical probiotics, topical hydroquinone, retinoids, bakuchiol, vitamin C, or acetyl zingerone containing products for two weeks to meet the washout criteria prior to enrolling.
- Subjects with any of the following facial cosmetic treatments in the past 3 months or those who are unwilling to withhold the following facial cosmetic treatments during the study including botulinum toxin, injectable fillers, microdermabrasion, intense pulsed light (IPL), peels, laser treatments, acid treatments, facial plastic surgery, or any other medical treatment administered by a physician or skin care professional which is designed to improve the appearance of facial skin.
- Individuals who have changed any of their hormonal based contraception within 3 months prior to joining the study.
- Current tobacco smoker or a tobacco smoking history of greater than 10 pack-years.
- Any known allergy to any of the ingredients in the study product.
- Those who have been on an oral antibiotic within 1 month prior enrolling
- Those who are unwilling to discontinue oral probiotics-based supplementation or supplement ingredients found in the study's oral, product 1 month prior to enrollment
Key Trial Info
Start Date :
December 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2024
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT06146140
Start Date
December 1 2023
End Date
December 1 2024
Last Update
November 24 2023
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