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Active clinical trials for "Dermatitis, Atopic"

Results 801-810 of 1075

Montelukast as a Controller of Atopic Syndrome

Seasonal Allergic RhinitisAllergic Conjunctivitis2 more

The purpose of the study is to find out if montelukast can be used to treat the various symptoms of allergic syndrome.

Completed10 enrollment criteria

Study of the Safety, Tolerability and Efficacy of BTX 1204 in Patients With Moderate Atopic Dermatitis...

Atopic Dermatitis

This is a randomized, double-blind, vehicle-controlled, Phase 2 study in subjects with moderate AD.

Completed43 enrollment criteria

In-Use Test With a Cosmetic Product

DermatitisAtopic

The aim of the study is to evaluate the tolerance of the product WO 4260 by a dermatologist. Additional objectives of this clinical in-use study are to evaluate the cosmetic features and acceptance of the product by means of a questionnaire in an interview situation and by skin hydration measurements on the scalp.

Completed14 enrollment criteria

Safety Study Evaluating the Adrenal Suppression Potential of Product 0405 in Pediatric Subjects...

Atopic Dermatitis

The aim of the trial is to assess Adrenal Suppression potential when pediatric subjects are administered Product 0405 for the treatment of Atopic Dermatitis

Completed4 enrollment criteria

Effect of Dietary Phospholipids on Atopic Dermatitis

DermatitisAtopic

The aim of the study is to investigate the influence of a milk phospholipid enriched dairy product on subjects with atopic dermatitis determining parameters of the immune status, the plasma lipid profile and the skin texture.

Completed11 enrollment criteria

Measuring Adherence to Topical Therapy in Children With Atopic Dermatitis and the Impact of a Return...

Atopic Dermatitis

The purpose of this research study is to better understand how the study drug works when people use it to treat atopic dermatitis.

Completed10 enrollment criteria

Validation of the Short-term Antimicrobial Action of Transplanted Bacteria

Atopic Dermatitis

Unlike healthy control skin, the skin of patients with atopic dermatitis (AD) is frequently colonized by Staphylococcus aureus (S. aureus), putting these patients at increased risk of S. aureus skin infections. In addition, research in the investigator's lab has shown that these patients have fewer protective antimicrobial Staphylococcal species such as Staphylococcal epidermidis (S. epidermidis) that are known to produce antimicrobial peptides that play a role in protecting the skin from invading pathogens. In this study, the investigator will attempt to decrease S. aureus colonization and increase colonization by protective Staph species in AD patients. First the investigator will capture the bacteria on subjects' lesional AD skin. Next the investigator will selectively grow the subject's antimicrobial Staphylococcal colonies and place them into a base moisturizer. The moisturizer plus bacteria will be applied to one of the subject's arms, and the moisturizer alone (without bacteria) to the other arm. The investigator will then do a quantitative wash of the bacteria growing on each arm one day later in order to determine whether the S. aureus abundance was affected by the application of the transplanted bacteria.

Completed19 enrollment criteria

Efalizumab for Eczema

DermatitisAtopic

The purpose of this study is to demonstrate a measurable improvement on a validated scale in a small population of adult patients with atopic dermatitis (eczema).

Completed17 enrollment criteria

A Study to Test Safety, Tolerability, and the Way the Body Absorbs, Distributes, and Gets Rid of...

HealthyAtopic Dermatitis

The clinical study consists of three parts: Part 1 with healthy volunteers. Part 2 and Part 3 including subjects with moderate to severe atopic dermatitis (a skin disease). For Part 1 the main goal of the study is to compare the safety, tolerability, and exposure of administration of the test drug via an injection in a skin layer just under the surface (subcutaneous), to administration of the test drug into the vein (intravenous). For Part 2 and Part 3 the main goal of the study is to assess the safety and tolerability of administration of the test drug via an injection in a skin layer just under the surface (subcutaneous) during 12 weeks of treatment.

Terminated22 enrollment criteria

Exploratory Study of the Cutaneous Penetration of Biodegradable Polymeric Microparticles in Atopic...

Atopic Dermatitis

This proof of concept study aims to assess in patients suffering from atopic dermatitis if polymeric microparticles reach the pilosebaceous follicles of inflamed skin.

Terminated37 enrollment criteria
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