The Cosmetic Effect of Mineral Clay Masks

University of California (UC) Davis

Status

Completed

Conditions

Rhytides

Treatments

Other: Clay mask

Study type

Interventional

Funder types

Other

Identifiers

NCT05041465

1296789

Details and patient eligibility

About

The aim of this study is to evaluate the cosmetic effects of commercially available mineral clay masks over a 4-week period. Changes in skin pigmentation, shine, wrinkles, and texture will be assessed.

A second aim of the study is to assess the safety and tolerability of mineral clay masks by assessing redness and participant feedback.

Enrollment

41 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Individuals aged 18-50
Individuals in good general health
Individuals free of any autoimmune or systemic disorder, which would interfere with the analysis.

Exclusion criteria

Individuals who have been on any topical prescribed medications for the past 2 weeks
Individuals who have history of acute or chronic disease that would likely interfere with or increase the risk on study participation at the discretion of the investigator
Individuals with active (flaring) disease or chronic skin allergies (atopic dermatitis/eczema) or those who have recently undergone treatment for skin cancer (within the last 12 months) in the area of testing on the forehead, nose and the cheeks
Female volunteers who are pregnant or planning to become pregnant over the course of the study. The risk to pregnant women is minimal but the facial appearance can be confounded by the altered hormones associated with pregnancy, as is well documented in chloasma which is dyspigmentation that arises in pregnancy. Women who become pregnant during the duration of the study will become ineligible but there are no birth control requirements.
Female volunteers who have started a new hormonal birth control agent or switched to a hormonal birth control agent within the past 60 days
Individuals who have had any medical or cosmetic procedure, such as laser resurfacing, or plastic surgery to the test site (face) within the last 6 months. This includes botulinum toxin, dermal fillers, collagen or other similar cosmetic procedure
Individuals who are currently using or during the past 14 days have used a retinoid such as tretinoin, adapalene, or retinol containing agents or a hydroquinone containing agent
Individuals who have used mineral clay masks on their face within the last 14 days
Individuals with a known history of hypersensitivity to any ingredients to the agent that is being assessed