Prospective Evaluation of Topical Almond Oil vs Hydroquinone
Study Details
Study Description
Brief Summary
The purpose of this study is to analyze facial pigmentation and skin microbiome changes after topical almond oil application, compared to the use of topical hydroquinone.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
The purpose of this experiment is to analyze facial pigmentation and skin microbiome changes after topical almond oil application, compared to the use of topical hydroquinone.
There will be a total of 50 subjects:
-
25 randomized to receive almond oil nightly
-
25 randomized to receive 2% hydroquinone nightly
Study Timelines:
-
The duration of an individual subject's participation will last from the day of the consent/screening (visit 1) until visit 5 where they will have images taken and measurements collected to assess skin pigment, skin hydration, sebum excretion rate.
-
The duration of participation is 4 months.
-
The estimated time for the investigators to complete primary analysis is 2 years.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Almond oil Almond Oil Pressed Cold |
Other: Almond Oil
Almond oil
|
| Active Comparator: Hydroquinone Hydroquinone 2% cream |
Drug: Hydroquinone Topical
Hydroquinone 2% cream
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Intensity of facial pigment [16 weeks]
Facial images will be obtained and analyzed with the BTBP image analysis system
Secondary Outcome Measures
- Shifts in the microbiome diversity (Shannon index as an example) [16 weeks]
The skin microbiome will be analyzed to assess any changes after topical almond oil application, compared to the use of topical hydroquinone.
- Quantification for the presence of species within the genus Cutibacteria, Staphyloccoccus, and Ralstonia [16 weeks]
The skin microbiome will be analyzed to assess the presence of species within the genus Cutibacteria, Staphyloccoccus, and Ralstonia
- Appearance of facial redness [16 weeks]
The research team will quantify the presence of facial redness with a SkinColorCatch from Delfin Technologies. This will measure the RGB colors and average them from each participant for each of the visits. Skin pigment, including the presence of redness, will be measured using a SkinColorCatch from Delfin Technologies. This device shows the RGB Colors, CIE L*a*b* and L*c*h* color space coordinates when the device is applied to the skin.Included is the link to the device (http://www.truesystem.co.kr/product/pdf/SkinColorCatch%20Brochure%202016.pdf).
- Subjective tolerability assessment [16 weeks]
A questionnaire that assesses for stinging, itching, and burning will be utilized.
- Intensity of facial pigment [8 weeks]
Facial images will be obtained and analyzed with the BTBP image analysis system
Eligibility Criteria
Criteria
Inclusion Criteria:
- Premenopausal women of Fitzpatrick skin types 3 to 6
Exclusion Criteria:
-
Those with a nut allergy
-
Smoking is an independent risk factor and serves as a confounder for the development of facial aging [18]. Therefore current smokers, those that have smoked within the past year, and former smokers with greater than a 20 pack year history of smoking will be excluded.
-
Those with an autoimmune photosensitive condition or a known genetic condition with a deficiency in collagen production (such as Ehlers-Danlos syndrome) will be excluded as this can be a confounder for facial photoaging.
-
Hormonal medications or therapies will not be allowed unless they have been stable on their medications for at least 2 months. Examples include oral contraceptives, progesterone-based injections, and estrogen based hormonal replacement therapy.
-
Those who have undergone any cosmetic procedures to the face in the 4 months prior to enrollment in the opinion of the investigator. People that have undergone deeper chemical peels (TCA based peels) within 1 year prior to enrollment will also not be eligible.
-
Individuals who are unwilling to discontinue vitamin E containing supplements and food sources during the washout and intervention.
-
Individual who are unwilling to discontinue topical cosmetic products during the duration of the study.
-
Individuals who are not willing to engage in a two-week washout on topical treatments known to affect facial pigmentation and these agents will be restricted during the study period as well. These include topicals that contain:
-
Retinoids such as tretinoin, adapalene, retinol.
-
Antioxidant ingredients such as vitamin C or vitamin E.
-
Pigment-reducing agents such as hydroquinone, azelaic acid, kojic acid per the discretion of the investigator except for the hydroquinone that is provided in this study.
-
Topicals that contain a nut oil or nut extract as part of their ingredient list.
-
Furthermore, subjects will be asked to refrain from use of any other topical products for one week prior to each visit apart from the study agents supplied from this study.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | UC Davis Department of Dermatology, Clinical Trials Unit | Sacramento | California | United States | 95816 |
Sponsors and Collaborators
- University of California, Davis
Investigators
- Principal Investigator: Raja Sivamani, MD MS AP, UC Davis Dermatology
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 1666478