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Dermatitis, Contact clinical trials

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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.

NCT ID: NCT00867607 Completed - Clinical trials for Allergic Contact Dermatitis

Safety, Tolerability, and Efficacy of 21 Days Dermal Application of MRX-6 on Mild to Moderate Contact Dermatitis

Start date: March 2011
Phase: Phase 1/Phase 2
Study type: Interventional

A Double-blind, Vehicle-controlled Study to Assess the Safety, Tolerability, and Efficacy of Three Weeks of Daily Dermal Application of MRX-6 or steroid on the Treatment of Mild to Moderate Allergic Contact Dermatitis of the Hand and Forearm. Total number of patients: up to 80.

NCT ID: NCT00824889 Completed - Melanoma Clinical Trials

Exploratory Study of Natural Killer Cells in Human Skin

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

Natural Killer (NK) cells play a unique role during innate immune responses as they are able to recognize and eliminate, without specific sensitization, tumors, microbe-infected cells as well as allogeneic cells.In a first time, we will characterize the tissue distribution, the phenotype and the effector functions of NK cells present in the human healthy skin.

NCT ID: NCT00795951 Completed - Dermatitis, Contact Clinical Trials

Clinical Evaluation of T.R.U.E. TEST in Children and Adolescents

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

Open, prospective, single-site, non-randomized study of the efficacy and safety of T.R.U.E. TEST allergens in children and adolescents ages 6-18.

NCT ID: NCT00779792 Active, not recruiting - Dermatitis, Contact Clinical Trials

Efficacy of Glycerol, Two Topical Steroids, and a Topical Immune Modulator Against Skin Irritation

WA+TR_1
Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy of glycerol ointment, triamcinolone acetonide ointment, clobetasol ointment and tacrolimus ointment on irritated skin in a cumulative skin irritation test model using healthy volunteers.

NCT ID: NCT00667056 Completed - Dermatitis Clinical Trials

Study of the Safety and Efficacy of Tacrolimus Ointment in Treating Chronic Allergic Contact Dermatitis

Start date: July 2004
Phase: Phase 4
Study type: Interventional

A study of subjects with a known nickel allergy comparing Tacrolimus to placebo, both associated with nickel patches to determine the safety and efficacy of treating Chronic Allergic Contact Dermatitis with Tacrolimus Ointment

NCT ID: NCT00646867 Completed - Contact Dermatitis Clinical Trials

Effect of Tetrix on Alleviation of Burning,Itching Associated With Lesions of Contact Dermatitis

Start date: February 2008
Phase: N/A
Study type: Interventional

To determine if Tetrix Cream, when applied to the skin lesions on patients with contact dermatitis, improves the symptoms of burning and itching.

NCT ID: NCT00643214 Completed - Healthy Clinical Trials

Evaluation of Tetrix Cream in the Healing of Injured Skin in Subjects With Contact Dermatitis

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

To determine if Tetrix Cream,, when applied to the skin lesions on patients with contact dermatitis, slows or interferes with the healing of the lesions.

NCT ID: NCT00640614 Completed - Contact Dermatitis Clinical Trials

Clinical Evaluation of T.R.U.E. TEST® : Safety and Efficacy

Start date: April 2008
Phase: Phase 3
Study type: Interventional

We propose an open, prospective, multi-center Phase III study to evaluate the diagnostic performance and safety of seven new T.R.U.E. Test allergens: Gold sodium thiosulfate, Hydrocortisone-17-butyrate, Bacitracin, Parthenolide, Methyldibromoglutaronitrile, Disperse blue 106, and Bronopol.Allergen performance and safety will be evaluated in adult patients with suspected contact dermatitis, and in adult patients with a known or suspected sensitization to at least one of the seven allergens.