Summary

Eligibility
for females ages 18 years and up (full criteria)
Location
at Sacramento, California
Dates
study started
estimated completion
Principal Investigator
by Raja K Sivamani, M.D.

Description

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.

Official Title

Prospective Evaluation of Topical Almond Oil vs Hydroquinone on the Appearance of Facial Pigmentation and the Stability of the Microbiome

Details

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.

Keywords

Skin Pigmentation Hydroquinone Almond Oil Hydroquinone Topical

Eligibility

You can join if…

Open to females ages 18 years and up

  • Premenopausal women of Fitzpatrick skin types 3 to 6

You CAN'T join if...

  • 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.

Location

  • UC Davis Department of Dermatology, Clinical Trials Unit accepting new patients
    Sacramento California 95816 United States

Lead Scientist at UC Davis

  • Raja K Sivamani, M.D.
    Associate Adjunct Professor, Dermatology. Authored (or co-authored) 130 research publications.

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Davis
Links
Sign up for this study
ID
NCT04875715
Phase
Phase 4
Study Type
Interventional
Last Updated