Vulvar Lichen Sclerosus Clinical Trial
Official title:
A Randomized Clinical Study Comparing Topical 0.05% Clobetasol Propianate in Vaseline With UVA-1 Phototherapy in the Treatment of Vulvar Lichen Sclerosus
Lichen sclerosus is a rare, chronic cutaneous disorder with a predilection for the genital
area. Any age group may be affected, although it is seen more often in postmenopausal women.
The current gold standard treatment is topical ultrapotent corticosteroids such as
clobetasol.
Here we compare UVA1 phototherapy with 0,05% clobetasol propionate in vaseline for the
treatment of vulvar lichen sclerosus.
Genital lichen sclerosus is a rare chronic inflammatory connective tissue disease. The
association with other autoimmune diseases and the detection of autoantibodies against ECM-1
point to an autoimmune genesis. Genital lichen sclerosus typically affects women around and
after the menopause. Common sites of affection are the vulva (clitoris and labia majora) and
the anus in women, the prepuce and the glans penis in men. Skin lesions include ivory-white,
atrophic, porcelain-like plaques with a tendency to atrophy and fissures in the advanced
stages.
First-line therapy for genital lichen sclerosus in the active, inflammatory phase is the use
of topical glucocorticoids. Alternatively, topically applied hormone-containing emollients
and topical calcineurin inhibitors are widely used. However, the use of topical
corticosteroids is because of the associated long-term side effects (atrophy, striae)
limited.
In the treatment of localized scleroderma (morphea), a similar sclerosing disease, the use
of ultraviolet radiation (UVA1) has proved highly effective. After a pilot study, the
high-dose UVA1 phototherapy (120 J / cm ²) was significantly more effective was a low-dose
UVA1 (20 J / cm ²), however no difference could be found in subsequent studies. Meanwhile,
the medium-dose UVA1 phototherapy in circumscribed scleroderma has been determined as the
most effective therapy regime and is included in the german dermatological guidelines (see
also AWMF guideline for diagnosis and therapy of circumscribed scleroderma at:
http://www.uni-duesseldorf.de/awmf/ll/013- 066.htm).
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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