Clinical Case Series Evaluating Skin Wellness System



Status:Completed
Conditions:Infectious Disease, Dermatology
Therapuetic Areas:Dermatology / Plastic Surgery, Immunology / Infectious Diseases
Healthy:No
Age Range:18 - Any
Updated:10/14/2017
Start Date:November 2012
End Date:June 2013

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An Open-Label Clinical Case Series to Demonstrate Efficacy of the Kendall Skin Wellness System

The purpose of this evaluation is to observe the performance of two (2) different skin care
treatment protocols on the skin:

#1 Kendall™ Body Wash & Shampoo in combination with the Moisture Barrier Cream; or #2
Kendall™ 2-in-1 Cleanser in combination with the Anti-fungal Cream.

The scientific evidence supports using these types of skin care products to keep the skin
healthy in the presence of moisture, urine, stool, or fungal infection. The cleansers are
preferred over soap and water and can be applied on all areas of the skin. The Moisture
Barrier Cream is formulated especially for skin exposed to moisture, urine, or stool. The
Antifungal Cream is utilized for fungal infections associated with athlete's foot, jock itch,
and ring worm to relieve itching, soreness, and irritation.

The Kendall™ Body Wash & Shampoo is a no-rinse cleanser that gently removed dirt, urine, and
stool while maintaining the natural pH of the skin (although it contains a shampoo
component); it can be applied on all areas of the skin. Kendall™ Moisture Barrier Cream
performs as a barrier to moisture and irritants when the natural barrier ability of the skin
has been compromised.

Kendall™ 2-in-1 Cleanser is a no-rinse cleanser that gently removes dirt, urine, and stool
and protects the skin from damage. Kendall™ Antifungal Cream is used on fungal infections to
relieve itching and discomfort.

Inclusion Criteria:

Adult subjects with any of the following indications:

- Erythema, maceration, or broken (denuded) skin from moisture, urinary or fecal
incontinence

- Irritated, unbroken skin (perineal area)

- Fungal infection present in the perineal area

Exclusion Criteria:

- An existing pressure ulcer of any stage where the product will be applied

- Subjects not expected to survive the two week trial

- Subjects under age 18

- Subjects unable to provide informed consent (or whose designated power of attorney is
unable to provide)

- Subjects with known sensitivity to any product preservative or other ingredient.
We found this trial at
2
sites
Southampton, Pennsylvania
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Southampton, PA
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Tucson, Arizona
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Tucson, AZ
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