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

NCT ID: NCT03093597

Last Updated: 2018-10-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

37 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-03-27

Study Completion Date

2017-12-12

Brief Summary

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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

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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.

Conditions

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Xerosis Xerosis Cutis Dry Skin; Eczema

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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virgin coconut oil

All subjects will apply virgin coconut oil to a previously randomize section of the skin on the left or right forearm.

Group Type ACTIVE_COMPARATOR

virgin coconut oil

Intervention Type OTHER

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.

virgin jojoba oil

All subjects will apply virgin jojoba oil to a previously randomize section of the skin on the left or right forearm

Group Type ACTIVE_COMPARATOR

virgin jojoba oil

Intervention Type OTHER

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.

virgin almond oil

All subjects will apply virgin almond oil to a previously randomize section of the skin on the left or right forearm

Group Type ACTIVE_COMPARATOR

virgin almond oil

Intervention Type OTHER

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.

white petrolatum ointment

All subjects will apply white petrolatum ointment to a previously randomize section of the skin on the left or right forearm.

Group Type ACTIVE_COMPARATOR

white petrolatum ointment

Intervention Type OTHER

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.

Interventions

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virgin coconut 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 coconut oil application twice daily for 2 weeks.

Intervention Type OTHER

virgin 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.

Intervention Type OTHER

virgin 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.

Intervention Type OTHER

white 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.

Intervention Type OTHER

Eligibility Criteria

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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.

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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of California, Davis

OTHER

Sponsor Role collaborator

University of Arizona

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Vivian Y Shi, MD

Role: PRINCIPAL_INVESTIGATOR

University of Arizona

Locations

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University of Arizona, Banner-University Medical Center

Tucson, Arizona, United States

Site Status

University of California, Davis

Sacramento, California, United States

Site Status

Countries

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United States

Other Identifiers

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1701110479

Identifier Type: -

Identifier Source: org_study_id

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