Skip to content

Evaluating the Effects of Cleansers on the Skin

Evaluating the Effects of Cleansers on the Skin

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03188653
Enrollment
20
Registered
2017-06-15
Start date
2017-05-31
Completion date
2020-05-31
Last updated
2021-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atopic Dermatitis

Brief summary

This will be a single visit study that will take approximately 2 hours. Up to 50 subjects (up to 25 healthy subjects, and up to 25 subjects with AD) from BUMC dermatology clinics will be enrolled in this study and randomized to receive the 7 cleansers on 7 test spots on their upper extremities. One spot will serve as a control and not receive any cleanser. Each spot will be cleansed with the corresponding cleanser for 15 seconds then rinsed off with tap water. Skin barrier will be measured at baseline, immediately after, 30, 60 and 90 minutes after rinse off.

Detailed description

Up to 50 subjects (up to 25 with healthy skin or 25 with atopic dermatitis) meeting the inclusion criteria will be enrolled in this study. A physical exam will be performed to ensure the subjects have healthy skin versus atopic dermatitis. For atopic dermatitis subjects, AD severity will be graded by the EASI score. Site randomization will be performed to determine which cleansers will be used for each of the 8 test sites (one site will be randomized to act as a control and not receive any cleanser). Baseline skin barrier function (TEWL, pH and hydration) will be measured. Then 1ml of each cleansers will be applied to the corresponding test sites, 2ml of tap water will be added, and lathered in a circular motion for 15 seconds. The sites will then be rinsed off with tap water for 15 seconds. Arms will be padded dry. Barrier functions will be measured again immediately after padding dry, and at 30, 60 and 90 minutes after.

Interventions

OTHERCeraVe® Eczema Soothing Body Wash

One of the 7 arm locations will be selected to receive CeraVe® Eczema Soothing Body Wash

OTHERCetaphil® RestoraDerm® Eczema Calming Body Wash

One of the 7 arm locations will be selected to receive Cetaphil® RestoraDerm® Eczema Calming Body Wash

OTHERDove® Sensitive Skin Body Wash

One of the 7 arm locations will be selected to receive Dove® Sensitive Skin Body Wash

OTHEREucerin® Skin Calming Body Wash

One of the 7 arm locations will be selected to receive Eucerin® Skin Calming Body Wash

OTHERAveeno® Skin Relief Body Wash

One of the 7 arm locations will be selected to receive Aveeno® Skin Relief Body Wash

OTHERMooGoo® Milk Wash

One of the 7 arm locations will be selected to receive MooGoo® Milk Wash

OTHERFree & Clear Liquid Cleanser

One of the 7 arm locations will be selected to receive Free & Clear Liquid Cleanser

Sponsors

University of Arizona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Male and female, at least 18 years of age Subject must be able to comprehend and read the English language. Healthy skin without concurrent atopic dermatitis or diagnosed with atopic dermatitis by a dermatologist

Exclusion criteria

Subjects who do not fit the inclusion criteria. Subjects unable to or unwilling to comply with the study procedures Concurrently have other inflammatory skin conditions. Prior known allergy to any components to of the cleansers tested A subject who, in the opinion of the investigator, will be uncooperative or unable to comply with study procedures. Subject unable to speak or read the English language, since all consents and instructions will be provided in English. Those that are prisoners or cognitively impaired

Design outcomes

Primary

MeasureTime frameDescription
Skin barrier function2 hoursTransepidermal water loss (TEWL) will be measured using hand-held, noninvasive skin barrier measuring device (VapoMeter).

Secondary

MeasureTime frameDescription
Skin barrier function2 hoursStratum corneum hydration status will be measured using hand-held, noninvasive skin barrier measuring device (MoistureMeterSC).
Skin pH2 hoursSkin pH will be measured.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026