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Dermatitis clinical trials

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NCT ID: NCT01125761 Withdrawn - Dermatitis Clinical Trials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NCT ID: NCT01045486 Withdrawn - Atopic Dermatitis Clinical Trials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NCT ID: NCT00871208 Withdrawn - Atopic Dermatitis Clinical Trials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NCT ID: NCT00746382 Withdrawn - Dermatitis Clinical Trials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.

NCT ID: NCT00378300 Withdrawn - Atopic Dermatitis Clinical Trials

The Effects of Probiotics in Atopic Dermatitis

Start date: July 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to study the clinical effects of taking probiotics in patients who have moderate to severe atopic dermatitis. There has been several studies showing improvement in the severity of atopic dermatitis after taking probiotics. The mechanism of this improvement is currently unknown. We propose that probiotics improve atopic dermatitis by stimulating, or increasing, the activity of a special type of cell called the T Regulatory cell--which can suppress the activity of allergic disease.

NCT ID: NCT00368719 Withdrawn - Atopic Dermatitis Clinical Trials

Evaluation to Assess the Long Term Safety of Tacrolimus Ointment for Atopic Dermatitis

Start date: September 2007
Phase: Phase 4
Study type: Interventional

To assess the long-term safety of tacrolimus ointment