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Eczema clinical trials

View clinical trials related to Eczema.

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NCT ID: NCT01652885 Completed - Dermatitis, Atopic Clinical Trials

Safety, Tolerability, and PK of AN2728 in Adolescents With Atopic Dermatitis

Start date: July 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate the safety, tolerability, and systemic exposure of AN2728 Topical Ointment, 2%, in subjects with atopic dermatitis.

NCT ID: NCT01639040 Completed - Atopic Dermatitis Clinical Trials

Study to Assess the Safety of Dupilumab (REGN668/SAR231893) Administered Concomitantly With Topical Corticosteroids (TCS) in Patients With Moderate-to-severe Atopic Dermatitis (AD)

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study was to assess the safety of Dupilumab administered concomitantly with topical corticosteroids (TCS) in patients with moderate-to-severe atopic dermatitis (AD).

NCT ID: NCT01638234 Completed - Atopic Dermatitis Clinical Trials

Effectiveness of Melatonin for Sleep Disturbances in Children With Atopic Dermatitis

Start date: January 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Sleep disturbance is a common complaint among patients with atopic dermatitis(AD). Melatonin may aid sleep and also has anti-inflammatory properties, and has been suggested in managing sleep disturbance in AD patients. However, there has been no large randomized controlled trials. Hence the objective of this double-blind randomized controlled study is to determine whether supplementing melatonin is effective in improving sleep problems in children with AD.

NCT ID: NCT01635738 Completed - Asthma Clinical Trials

Probiotics and Allergic Diseases

probiotics
Start date: December 2011
Phase: N/A
Study type: Interventional

Many studies had demonstrated that probiotics could be applied in the prevention and adjuvant treatment for allergic diseases. In this study, we investigate the effects of Lactobacillus paracasei GMNL-133(LP), Lactobacillus fermentum GM-090 (LF), and Lactobacillus paracasei GMNL-133(LP) with Lactobacillus fermentum GM-090 (LF) combination products used for adjuvant treatment of atopic dermatitis and asthma.

NCT ID: NCT01614756 Completed - Clinical trials for Healthy Subjects and Atopic Dermatitis Subjects

A Two-Part, Phase 1, Single-Dose Study of IL-31 mAb (Anti-Interleukin 31 Monoclonal Antibody); in Healthy Subjects and Adults With Atopic Dermatitis

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

The purpose of the study is to determine safety and tolerability of IL-31 mAB

NCT ID: NCT01602341 Completed - Dermatitis, Atopic Clinical Trials

Efficacy and Safety of AN2728 Topical Ointment to Treat Adolescents With Atopic Dermatitis

Start date: August 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of AN2728 Topical Ointment, 2% and 0.5%, administered once a day (QD) or twice a day (BID), in the treatment of adolescents with atopic dermatitis (AD)

NCT ID: NCT01597817 Completed - Atopic Dermatitis Clinical Trials

Efficacy and Safety of a a Biofunctional Textile in the Management of Atopic Dermatitis

2ndDermisII
Start date: November 2011
Phase: Phase 2
Study type: Interventional

Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by exacerbations and remission of intensely pruritic lesions of variable location. AD may be acute (short-term and severe) with predominantly redness, vesicles and oozing, or it may be chronic (long-term) with scaling, skin thickening, altered pigmentation and exaggerated surface markings. The condition affects mainly the creases of the elbows and knees, and the face and neck, although it can affect any part of the body. The severity of AD is variable, ranging from localized mild scaling to generalized involvement of the whole body. Itching is the predominant symptom, which can induce a vicious cycle of scratching, leading to skin damage. There is a tendency to lifelong dry sensitive skin. Skin of AD is often colonized by Staphylococcus aureus contributing to perpetuating cutaneous inflammation. AD treatment is based on skin hydration, identification and elimination of flare factors, and pharmacologic therapy. Biofunctional textiles are emerging as new and complementary tools . Chitosan is a natural polysaccharide with in vitro anti-microbial activity and regenerating properties. The investigators aim to evaluate the effect of a textile coated with chitosan in AD treatment as well as its impact on systemic inflammation and skin microbiome. The investigators hypothesize the use of biofunctional textile coated with chitosan will improve severity of AD , quality of life and diminish skin colonization with Staphylococcus aureus and some skin moulds, namely Malassezia.

NCT ID: NCT01591785 Completed - Hand Eczema Clinical Trials

Treatment of Staphylococcus Aureus Colonization in Hand Eczema

Start date: January 2012
Phase: N/A
Study type: Interventional

Atopic dermatitis is a chronic disease characterized by itching and eczematous lesions. In adults, eczema commonly localizes to the hands or feet. Several studies have implicated bacterial contamination, especially with Staphylococcus aureus (S. aureus), to be a factor in atopic dermatitis, as infection with this bacteria correlates with disease severity. No trial to date has investigated how to treat S. aureus infection in adults with hand or hand/foot dermatitis. Using retapamulin ointment in the nose and on the hands or hands/feet, the investigators expect to have a significant clearance rate of s. aureus infection. The investigators believe that treating the bacterial infection along with treating the condition with a topical corticosteroid will significantly decrease the severity of hand/foot dermatitis in our study population.

NCT ID: NCT01591070 Completed - Clinical trials for Seborrheic Dermatitis

Proactive Treatment of Tacrolimus Ointment for Adult Facial Seborrheic Dermatitis

Start date: November 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether proactive use of 0.1% tacrolimus ointment once or twice weekly can keep adult facial SD in remission and reduce the incidence of exacerbation.

NCT ID: NCT01569906 Completed - Clinical trials for Moderate to Severe Atopic Eczema

Narrowband UVB for Children With Moderate to Severe Atopic Eczema

Start date: April 2009
Phase: N/A
Study type: Observational

To assess prospectively, the response of moderate to severe atopic eczema to a standard course of narrowband ultraviolet B phototherapy by using validated objective and subjective scoring systems.