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Up to: Inflammatory disease · Vascular disorder
Vasculitis
Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. Behcet disease) to relatively minor skin disease.
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Necrotizing vasculitis 0 trials · 143 incl. sub-types Sub-types →
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Arteritis 5 trials · 104 incl. sub-types Sub-types →
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Central nervous system vasculitis 3 trials · 55 incl. sub-types Sub-types →
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Phlebitis 13 trials · 21 incl. sub-types Sub-types →
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Immune complex mediated vasculitis 0 trials · 18 incl. sub-types Sub-types →
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Hypersensitivity vasculitis 0 trials · 16 incl. sub-types Sub-types →
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Kawasaki disease 15 trials
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Cutaneous vasculitis 4 trials · 5 incl. sub-types Sub-types →
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Deficiency of adenosine deaminase 2 3 trials
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Retinal vasculitis 2 trials
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Aortitis 1 trial
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Livedoid vasculopathy 1 trial
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Choroiditis 0 trials · 1 incl. sub-types Sub-types →
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Secondary vasculitis 0 trials · 1 incl. sub-types Sub-types →
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Shwartzman phenomenon 0 trials
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Autoimmune vasculitis 0 trials Sub-types →
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Lymphangitis 0 trials
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Vasculitis, lymphocytic, nodular 0 trials