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Effect of moisturizing creams on skin barrier function and prevention of Malassezia recurrence in patients with atopic eczema

Conditions
Dry skin barrier disorders such as atopic eczema and ichtyosis
Registration Number
EUCTR2008-000552-27-SE
Lead Sponsor
ACO HUD NORDIC AB
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

•Dry skin barrier disorders such as atopic dermatitis (Patientgroup 1)
•Malassezia eradicated head and neck dermatitis (Patientgroup 2)
•Rough or clinically normal skin on the volar aspect of the forearm
•Either gender
•Age between 18 and 65 years
•Written Informed Consent
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•Possible allergy to ingredients in the study medications
•Use of any concomitant medication that may interfere with the study related activities or assessment of efficacy
•Any patient related factor suggesting potential poor compliance with study procedures (e.g. psychiatric disorders, history of alcohol or substance abuse)
•Any serious medical condition which, in the opinion of the investigator, may interfere with the evaluation of the results
•Pregnancy or breast feeding, or patients who plan to become pregnant during the course of the study

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: •To compare the effect from a new active emulsion and its placebo on skin barrier function ;Secondary Objective: •To compare the effect from a new active emulsion and a reference cream on skin barrier function for Malassezia patients <br>•To compare the influence of new active treatment with placebo and new active treatment with reference on Malassezia recurrence <br>•To study the degree of adverse skin reactions (stinging)<br>•To study the willingness to pay for a treatment not inducing stinging at application.<br>•To study the skin hydrating effect of the creams <br>•To evaluate cosmetic variables of the creams <br><br>;Primary end point(s): •skin susceptibility to irritation from an irritating agent measured as transepidermal water loss (TEWL) after treatment with new active emulsion and its placebo<br><br>The skin barrier function measured as TEWL prior to application of irritating agent is supportive to the primary variable
Secondary Outcome Measures
NameTimeMethod
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