Cutaneous Lupus Erythematosus, Experimental Photoinduction, Protective Sunscreen, Skin Lesion
Conditions
Keywords
cutaneous lupus erythemaosus, photoprotection, photoprovocation, Sunscreen RV 2547C
Brief summary
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.
Interventions
DRUGsunscreen RV 2547C
Sponsors
Heinrich-Heine University, Duesseldorf
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Male or female subjects * Patient aged of 18 years or more * Documented medical history of chronic cutaneous lupus erythematosus (lupus erythematosus tumidus, discoid lupus erythematosus, subacute lupus erythematosus) without any sign of systematic involvement * patients who have a history of positive provocative phototestimg using a standardized protocol during a previous photobiologic exploration * informed consent
Exclusion criteria
* Pregnant women, nursing mothers * subjects with lupus erythematosus with systematic involvement * subjects with a medical history of another photodermatosis * subjects with sun erythema, residual pigmentation, dermatological lesion, abnormal skin pigmentation which might interfere with a study evaluation on test sides * subjects who had sun solar simulator exposure on their backs within 12 weeks prior to enter to the study * subjects with a known intolarance to one of the formula compounds
Countries
Germany
Outcome results
None listed