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Skin Barrier Biophysical Properties and Clinical Appearance After Moisturizer in Dry Skin

Evaluating Skin Barrier Biophysical Properties and Clinical Appearance After Moisturizer Use in Patients With Dry Skin

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03093597
Enrollment
37
Registered
2017-03-28
Start date
2017-03-27
Completion date
2017-12-12
Last updated
2018-10-11

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

Conditions

Xerosis, Xerosis Cutis, Dry Skin; Eczema

Brief summary

The purpose of the study is to compare the changes in the appearance of dry skin after the use various moisturizers: white petrolatum ointment, coconut oil, jojoba oil, and almond oil in patients with dry skin.

Detailed description

The goal of this study is to compare how the appearance of dry skin changes before and after the use of following moisturizers: white petrolatum, coconut oil, jojoba oil and almond oil). Up to 40 subjects from Banner-University Medical Center/University of Arizona dermatology clinics and University of California, Davis dermatology clinics (up to 20 subjects per site) who have dry skin will be enrolled in this study and randomized to receive the four moisturizers on four locations on their forearms.There will be a total of 3 study sessions: baseline, and approximately 1 and 2 weeks for follow up assessment. At each visit, dry skin severity will be evaluated by a trained observer using a validated Dry Skin Score, skin barrier biophysical properties (transepidermal water loss and hydration) will be measured, and digital photos of the test sites will be taken for image analysis.

Interventions

One of the four locations (right proximal forearm, right distal forearm, left proximal forearm, left distal forearm) on the forearm will be selected to receive virgin coconut oil application twice daily for 2 weeks.

OTHERvirgin jojoba oil

One of the four locations (right proximal forearm, right distal forearm, left proximal forearm, left distal forearm) on the forearm will be selected to receive virgin jojoba oil application twice daily for 2 weeks.

OTHERvirgin almond oil

One of the four locations (right proximal forearm, right distal forearm, left proximal forearm, left distal forearm) on the forearm will be selected to receive virgin almond oil application twice daily for 2 weeks.

OTHERwhite petrolatum ointment

One of the four locations (right proximal forearm, right distal forearm, left proximal forearm, left distal forearm) on the forearm will be selected to receive white petrolatum ointment application twice daily for 2 weeks.

Sponsors

University of California, Davis
CollaboratorOTHER
University of Arizona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

1. Male and female, at least 18 years of age 2. Subject must receive a diagnosis of dry skin by a dermatologist. 3. Subject must be able to comprehend and read the English language.

Exclusion criteria

1. Subjects who do not fit the inclusion criteria. 2. Subjects unable to or unwilling to comply with the study procedures 3. Prior known allergy to white petrolatum, coconut oil, almond oil, or jojoba oil. 4. People who have used products containing white petrolatum, jojoba oil, coconut oil, or almond oil within the past week. 5. People with a known diagnosis of ichthyosis. 6. A subject who, in the opinion of the investigator, will be un-cooperative or unable to comply with study procedures. 7. Subject unable to speak or read the English language, since all consents and instructions will be provided in English. 8. Those that are prisoners or cognitively impaired

Design outcomes

Primary

MeasureTime frameDescription
The appearance of xerosis14 daysThe clinical severity of xerosis of the 4 location will be graded by a trained observed using a previously validated Dry Skin Scale and by analysis of the digital photos.

Other

MeasureTime frameDescription
Skin barrier biophysical properties of xerosis14 daysTransepidermal water loss (TEWL) and stratum corneum hydration status will be measured using hand-held, noninvasive, skin barrier measuring devices (Tewameter and moistureMeter)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026