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Dermatitis, Atopic clinical trials

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NCT ID: NCT01695707 Withdrawn - Atopic Dermatitis Clinical Trials

Assessing the Impact of Pioglitazone on Skin Barrier Function in Atopic Dermatitis Patients

Start date: March 2013
Phase: N/A
Study type: Interventional

Many patients with eczema (atopic dermatitis) have an inherent defect in their skin barrier as demonstrated by high water loss. In laboratory conditions, studies have shown that pioglitazone restores the skin barrier function in skin from eczema patients. The purpose of this study is to determine if taking pioglitazone improves the skin barrier function in people with eczema.

NCT ID: NCT01691209 Withdrawn - Dermatitis, Atopic Clinical Trials

Efficacy/Safety Study to Explore a New Topical Formulation in Atopic Dermatitis

Phoenix
Start date: October 2013
Phase: N/A
Study type: Interventional

The study shall explore whether treatment of atopic dermatitis is equally effective with Phoenix medical device as compared to standard therapy (Hydrocortisone cream).

NCT ID: NCT01385527 Withdrawn - Atopic Dermatitis Clinical Trials

Pediatric Atopic Dermatitis (AD) Internet Survey

Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether participation in an Internet-based intervention helps improve atopic dermatitis treatment outcomes.

NCT ID: NCT01368315 Withdrawn - Atopic Dermatitis Clinical Trials

CT 327 in the "Atopy Patch Test" Model

CT327 AD01-09
Start date: n/a
Phase: Phase 1
Study type: Interventional

A Randomized, Double-Blind, Phase I, Single-Center Study on the Efficacy and Safety of CT 327 in the Atopy Patch Test model.

NCT ID: NCT01230190 Withdrawn - Atopic Dermatitis Clinical Trials

Management of Eczema by Specific Probiotic Strains

BAMBOO
Start date: March 2011
Phase: Phase 3
Study type: Interventional

To investigate the therapeutic effect of a selected probiotic mixture on the severity of AD in infants aged 0-15 months. The probiotic mixture has been studied in laboratory setting and has proven IL-10 stimulating effects. Therefore it is thought to decrease AD severity in young children (beyond the conventional treatment).

NCT ID: NCT01125761 Withdrawn - Dermatitis Clinical Trials

Efficacy and Safety of the Association Drugs in Patients With Allergic Dermatitis

Start date: November 2010
Phase: Phase 3
Study type: Interventional

Considering the pathogenesis of several allergic skin diseases to be investigated in this study as well as the pharmacodynamic mechanisms of the association of dexamethasone and clemastine fumarate, it is believed that the components of topical medication may act synergistically in the reduction of signs and symptoms of the diseases in question. Therefore it is expected that the association promotes results significantly superior to dexamethasone alone.

NCT ID: NCT01045486 Withdrawn - Atopic Dermatitis Clinical Trials

the Effectiveness of Probiotics on Atopic Dermatitis With Cow Milk Allergy

Start date: January 2010
Phase: N/A
Study type: Interventional

There is not enough evidence to support the use of probiotics for prevention or treatment of AD in children in clinical practice. The purpose of this study is to determine whether probiotics is effective in the treatment of atopic dermatitis with cow milk allergy.

NCT ID: NCT00871208 Withdrawn - Atopic Dermatitis Clinical Trials

Trial of Treatment of Atopic Dermatitis With Concurrent Altabax® and Topical Low-Potency Corticosteroids Versus Low-Potency Corticosteroid Mono-therapy

Start date: May 2009
Phase: Phase 4
Study type: Interventional

This study is designed to determine whether the addition of topical Altabax (R) to a treatment regimen of topical corticosteroid therapy speeds clearance of atopic dermatitis and improves quality of life.

NCT ID: NCT00746382 Withdrawn - Dermatitis Clinical Trials

A Placebo Controlled 4 Week Proof of Concept Study With 0.5% Roflumilast Cream in Patients With Mild Atopic Dermatitis (RO-2351-001-EM)

Start date: November 2008
Phase: Phase 2
Study type: Interventional

The aim of this proof of concept study is to show the safety and efficacy of 0.5 % dermal roflumilast cream in the treatment of atopic dermatitis in adults. This is a multicenter, randomized, double-blind, placebo-controlled, parallel group study. 2-5 % of the body surface area (BSA) should be covered with a mild form of atopic dermatitis. In a 4-week treatment period 38 mg cream is applied two times daily on 0.5 to 1 % of the BSA. After a screening phase, a washout phase of flexible duration (max 30 days, time depending upon pre-medication), the 28 day treatment phase follows.As roflumilast is a potent antiinflammatory substance, a positive effect on this form of dermal disease is anticipated.

NCT ID: NCT00389103 Withdrawn - Atopic Dermatitis Clinical Trials

Safety Study of MVA Smallpox Vaccine in Subjects With a History of Atopic Dermatitis (AD)

Start date: October 2006
Phase: Phase 1
Study type: Interventional

purpose of this study is to assess the safety and immunogenicity of two MVA smallpox vaccine injections in healthy adults that are 18-35 years of age with a history of mild to moderate Atopic Dermatitis.