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Dermatitis, Contact clinical trials

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NCT ID: NCT02028182 Completed - Contact Dermatitis Clinical Trials

Clinical Evaluation of Lyral® Dose Response Study

Start date: February 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine optimal allergen dose as the lowest concentration eliciting positive reactions in 70-90% of subjects. Frequency of positive, negative, doubtful and irritant reactions, and concordance with a corresponding reference allergens will be captured.

NCT ID: NCT01798589 Completed - Clinical trials for Allergic Contact Dermatitis

Bioequivalence of Ethylenediamine Dihydrochloride Study

Start date: July 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the allergen ethylenediamine dihydrochloride when prepared using methylcellulose versus preparation using polyvinylpyrrolidone.

NCT ID: NCT01797562 Completed - Clinical trials for Allergic Contact Dermatitis

Clinical Evaluation of T.R.U.E. Test Allergens in Children an Adolescents

Start date: December 10, 2012
Phase: N/A
Study type: Interventional

The objective of the study was to evaluate the diagnostic performance and safety of T.R.U.E. Test allergens in pediatric subjects aged 6-17 years old. In total, 11 allergens were evaluated; 7 new allergens on panels 2.2 and 3.2 and 4 previously approved allergens for which changes were made to dose and excipient.

NCT ID: NCT01546298 Completed - Clinical trials for Allergic Contact Dermatitis

Immune Reactions in Contact Dermatitis Affected Skin

Start date: January 2012
Phase:
Study type: Observational

This study hopes to improve the investigators understanding of how the immune system acts in allergic contact dermatitis. In order to reach this goal, normal volunteers, who are suspected of having allergic contact dermatitis, will be patch tested for the fifteen most common allergens. Then, biopsies will be taken of the skin at the sites where the there is a positive reaction to the allergen. Also, small biopsies will be taken from an area that received a patch but no allergen and an area that did not receive a patch to serve as controls. In a second stage of the study, volunteers will receive patches with the allergen to which they demonstrated an allergic response. More biopsies will be taken, over three designated time points. The biopsied skin samples will then be studied in a laboratory.

NCT ID: NCT01529320 Completed - Clinical trials for Allergic Contact Eczema

Assess Itch Behavior in Nickel Sulphate Sensitized Volunteers

Start date: February 2012
Phase: Phase 1
Study type: Interventional

Determine the mean time to itch relief from the start of treatment with topic methylprednisolone aceponate.

NCT ID: NCT01244607 Completed - Clinical trials for Allergic Contact Dermatitis

NI-0801 in Allergic Contact Dermatitis

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess the effect of a single dose of NI-0801 on the severity of nickel-induced allergic contact dermatitis.

NCT ID: NCT00931242 Completed - Atopic Dermatitis Clinical Trials

Study of Apremilast in Atopic or Contact Dermatitis

Start date: June 2009
Phase: Phase 2
Study type: Interventional

The objective of this study is to evaluate the efficacy of apremilast in patients with recalcitrant atopic or contact dermatitis.

NCT ID: NCT00929981 Completed - Dermatitis, Contact Clinical Trials

A Study To Assess Safety And Effectiveness Of Medrol In Contact Dermatitis In Indian Patients

Start date: September 2009
Phase:
Study type: Observational

This study will be a prospective, non-interventional, single arm and open label study, in patients with contact dermatitis requiring systemic steroid therapy with a purpose to obtain the real life effectiveness and tolerability of Medrol in treating contact dermatitis in Indian patients. Patients with contact dermatitis who have been prescribed for Medrol will be enrolled into the study and will be followed up for the resolution of symptoms

NCT ID: NCT00928447 Completed - Clinical trials for Dermatitis, Allergic Contact

Study of the Intradermal Injection of rHuPH20 or Placebo in Participants With Nickel Allergic Contact Dermatitis

Start date: June 23, 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effect and safety of rHuPH20 or placebo for the prevention and treatment of skin allergic reaction to nickel. The study drug and placebo will be administered by intradermal injection.

NCT ID: NCT00871052 Completed - Clinical trials for Polymorphic Light Eruption

Calcipotriol and Polymorphic Light Eruption

Start date: March 2009
Phase: N/A
Study type: Interventional

Polymorphic light eruption (PLE) is a photodermatosis with an extremely high prevalence, particularly among young women (up to 20%). The disease is characterized through itchy skin lesions on sun-exposed body sites occurring after sun exposure mostly in spring and early summer. Its etiopathogenesis is unknown but resistance to ultraviolet radiation (UVR)-induced immunosuppression with subsequent immune reactions against skin photoneoantigens has been suggested. The phenomenon of UVR-induced immunosuppression (suppression of CHS) has been well known for many years. Recent findings showed that regulatory T cells (CD4+CD25+FoxP3+) (Tregs), a subset of T helper cells, are crucial in UVR-induced immunosuppression. However, the requirements for the maintenance of peripheral CD4+CD25+ T cells, important in suppression of immune responses, are still incompletely understood. Recent work suggests that cutaneous RANKL might be the physiologic missing link that couples UVR to immunosuppression. Epidermal RANKL, expressed in keratinocytes of inflamed skin due to e.g. UVR exposure was shown to control the number of Tregs via activation of dendritic cells, hereby mediating UVR-induced immunosuppression (e.g. suppression of allergic contact hypersensitivity responses). In addition to the suppression of local cutaneous hyperallergic responses, the development of systemic autoimmunity is suppressed. A strong inducer of RANKL expression and of Tregs is vitamin D3 that has been reported to have immunosuppressive effects. Interestingly, patients with autoimmune disorders (e.g. lupus erythematosus) may exhibit reduced vitamin D3 blood levels. This randomized, double blinded left-right body side experimental comparison study was designed to assess the preventive effect of the vitamin D3 analogue calcipotriol in patients with PLE. The hypothesis is tested that treatment with a calcipotriol-containing cream can prevent the UVR-induced development of PLE skin lesions. Better insight into the pathogenesis of PLE may give clues to develop new therapeutic strategies.