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Atopic Dermatitis clinical trials

View clinical trials related to Atopic Dermatitis.

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NCT ID: NCT00693693 Completed - Atopic Dermatitis Clinical Trials

Adherence to Topical Hydrocortisone 17-butyrate 0.1% (Locoid®) Using Different Vehicles in Adults With Atopic Dermatitis

Start date: November 2006
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to better understand adherence to Locoid when people use it to treat atopic dermatitis.

NCT ID: NCT00691366 Completed - Atopic Dermatitis Clinical Trials

Comprehensive Investigation of Heart Rate Variability as a Measure of the Autonomic Nervous System in Atopic Dermatitis

Start date: March 2007
Phase: N/A
Study type: Observational

The purpose of this research is to study heart rate patterns in people with moderate to severe atopic dermatitis and how itching affects those patterns.

NCT ID: NCT00690833 Completed - Atopic Dermatitis Clinical Trials

Efficacy of Desonide (Desonatetm) Gel 0.05% in Younger and Older Subjects With Atopic Dermatitis

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

The purpose of this research study is to better understand how this study drug works when people use it to treat atopic dermatitis. Desonate has been approved by the US Food and Drug Administration (FDA) for atopic dermatitis.

NCT ID: NCT00690807 Completed - Atopic Dermatitis Clinical Trials

A Phase 2 Study of PH-10 for the Treatment of Atopic Dermatitis

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

PH-10 is a formulation of rose bengal disodium (RB) for topical administration to the skin. PH-10 is capable of undergoing photochemical reactions when activated by ambient light. This phase 2 study will assess whether topical PH-10 applied once daily to mild, moderate or severe areas of atopic dermatitis (including atopic eczema) may ameliorate inflammation of the skin when activated by ambient light.

NCT ID: NCT00660127 Completed - Atopic Dermatitis Clinical Trials

The Effect of Visual Stimuli on Itch Perception Intensity in Healthy and Atopic Dermatitis Patients

Start date: October 2007
Phase: N/A
Study type: Observational

The purpose of this research study is to assess whether seeing other people itch affects itch perception in patients with atopic dermatitis and healthy subjects.

NCT ID: NCT00654355 Completed - Atopic Dermatitis Clinical Trials

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

Start date: April 2008
Phase: Phase 4
Study type: Interventional

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

NCT ID: NCT00616538 Completed - Atopic Dermatitis Clinical Trials

Epiceram™ Device Versus Mid-Strength Topical Steroid (Fluticasone Propionate 0.05%) for Treatment of Atopic Dermatitis

Start date: December 2006
Phase: Phase 4
Study type: Interventional

Novel therapies for AD that avoid immunosuppression and potential carcinogensis are needed. EpiCeram™ , a topical cream, represents a novel class of therapy for skin disorders that does not contain corticosteroids or other anti-inflammatory drugs. The objective of the present study is to demonstrate the safety and efficacy of EpiCeram ™ in the treatment of moderate to severe atopic dermatitis as compared to mid-strength topical steroid cream following twice daily dosing for four weeks in pediatric patients with AD. The potential benefit to patients lies in the potential for EpiCeram ™ to provide restoration of the normal skin barrier as shown in previous studies and eliminate or reduce the requirement for supplemental topical steroid administration.

NCT ID: NCT00614731 Completed - Atopic Dermatitis Clinical Trials

Responses to Immunization With Keyhole Limpet Hemocyanin Administered by Scarification and the Intradermal Route

Start date: December 2007
Phase: Phase 1
Study type: Interventional

Atopic dermatitis (AD) is a skin disorder in which people often have swelling and skin infections. People with this disease cannot receive the smallpox vaccine because it could cause them to have a fatal reaction known as eczema vaccinatum (EV). Keyhole limpet hemocyanin (KLH) is a protein that can be used to deliver vaccines to the body. The purpose of this study is to determine a baseline immune reaction to KLH in people without AD. Once this has been established, other studies can be designed to determine whether KLH can be used to give vaccines to people with AD.

NCT ID: NCT00610142 Completed - Atopic Dermatitis Clinical Trials

Comparison of Atrophogenic Effect of Hydrocortison 1% Cream and Pimecrolimus 1% Cream Assessed by Optical Coherence Tomography (OCT) and 20-MHz Ultrasound of Uninvolved Skin in Patients With Atopic Dermatitis

OCT-AD
Start date: December 2007
Phase: Phase 2
Study type: Interventional

to explore the atrophogenic potentials of hydrocortison 1% cream and pimecrolimus 1% cream on unaffected forehead skin

NCT ID: NCT00557284 Completed - Atopic Dermatitis Clinical Trials

Efficacy Study of Montelukast in Atopic Dermatitis Induced by Food Allergens

Start date: March 2008
Phase: Phase 4
Study type: Interventional

AD is a disease found in children; the focus of the study is the mechanisms associated in children with AD induced by food allergies. This study will be a randomized, double-blind, placebo-controlled, parallel group trial conducted in participants diagnosed with atopic dermatitis and food allergies. The study duration for participants will be approximately 9 weeks. A total of 20 participants will be recruited for the entire study. Each arm will consist of 10 participants.The study will enroll 20 children, male or female, 1 - 8 years of age with atopic dermatitis (AD) associated with food allergens, previously documented by skin or RAST test, before enrollment. Atopic dermatitis and gastrointestinal (GI) symptoms will be scored and followed throughout the study.