Clinical Trials Logo

Lupus Erythematosus, Cutaneous clinical trials

View clinical trials related to Lupus Erythematosus, Cutaneous.

Filter by:

NCT ID: NCT01146444 Completed - Clinical trials for Cutaneous Lupus Erythematosus

Sunscreens in Patients With Cutaneous Lupus Erythematosus(CLE)

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

Part I: to investigate the efficacy of different sunscreens in the prevention of skin lesions following standardized photoprovocation with Ultraviolet A/Ultraviolet B (UVA/UVB) light in patients with CLE. Part II: to evaluate the influence of different sunscreens on the expression of biomarkers in the skin of patients with CLE and of Healthy Controls following UV irradiation.

NCT ID: NCT00633945 Completed - Clinical trials for Cutaneous Lupus Erythematosus (CLE)

Evaluation of Lenalidomide (REVLIMID®) to Treat Subjects With Cutaneous Lupus Erythematosus (CLE)

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

This study is being conducted to evaluate the safety and effectiveness of lenalidomide (Revlimid®) in subjects with Cutaneous Lupus Erythematosus (CLE). The study drug will be used in an off-label indication to treat 6 subjects for 12 months each. Men and women over the age of 18, who have a biopsy proven diagnosis of CLE and who have failed standard treatment, will be included in the study.

NCT ID: NCT00523588 Completed - Clinical trials for Cutaneous Lupus Erythematosus

Treatment of Cutaneous Lupus Erythematosus (CLE) With the 595 nm Flashlamp Pulsed Dye Laser

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The purpose of using the 595 nm Vbeam Perfectaâ„¢ flashlamp-excited, pulsed dye laser in this study is to help improve study patients' skin disease. Cutaneous lupus erythematosus (CLE) often presents with disfiguring vascular lesions which are frequently difficult to treat with the available therapeutic measures, such as photoprotection, topical steroids, and antimalarials. Laser therapy provides an alternative treatment option for CLE patients. Although there has been documented experience with laser treatment in CLE patients, no study comparing treated lesions to the natural course of the disease has been conducted.

NCT ID: NCT00470912 Completed - Skin Lesion Clinical Trials

Sunscreen RV 2457C in Photoinduced CLE

Start date: May 2001
Phase: Phase 3
Study type: Interventional

Lupus erythematosus (LE) is characterized by a large clinical spectrum, and sunligt is a well established factor in the induction and exacerbation of this disease. In all subsets of LE, skin lesions occur preferentially in sun-exposed areas. Previous studies have demonstrated that the lesions in LE patients reproduced in controlled experimental conditions. The initial reports suggested that the action spectrum for the LE was in the UVB range (290 to 320 nm), but more recent studies have demonstrated that UVA (320 to 400 nm) can contribute to the induction of LE skin lesions. Antimalarial agents and topical steroids are the main treatments of chronic LE. The second line therapies include retinoids, sulfones, immunosuppressor agents, systemic corticosteroid and thalidomide. Moreover, patients are advised to avoid sun, to wear sunprotective clothing and to apply sunscreen. The aim of this study was to assess the efficacy of a sunscreen milk with high protection factor against UV-B and UV-A, used exclusively, in the photoinduced LE.

NCT ID: NCT00420173 Completed - Clinical trials for Cutaneous Lupus Erythematosus

Interdisciplinary Study Group of Lupus Erythematosus (ISGLE)

Start date: September 2004
Phase: N/A
Study type: Observational

Cutaneous lupus erythematosus (CLE) is a disease with a wide spectrum of clinical manifestations and a variable prognosis. The aim of this study is to create a standardized evaluation of the different subtypes of this disease in order to receive an overview of the spectrum of clinical and laboratory features as well as the therapeutic strategies for patients with CLE.

NCT ID: NCT00317681 Completed - Clinical trials for Cutaneous Lupus Erythematosus

Efficacy of Topical Tacrolimus in Different Subtypes With Cutaneous Lupus Erythematosus (CLE)

Start date: August 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of topical tacrolimus in different subtypes of cutaneous lupus erythematosus. As shown by several groups activated memory T lymphocytes play a key role in the pathogenesis of lupus erythematosus. Tacrolimus targets T lymphocytes and suppresses their activation by inhibiting the expression of cytokine genes, such as IL-2. Therefore, treatment of cutaneous lupus erythematosus with topical tacrolimus might result in an improvement of skin lesions in such patients.