Phase
Condition
Polymyalgia Rheumatica (Pmr)
Collagen Vascular Diseases
Connective Tissue Diseases
Treatment
N/AClinical Study ID
Ages > 50 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Decreased visual acuity (BVA) <5 days, regardless of degree of severity, abrupt onsetin the context of newly diagnosed or suspected Horton's disease at this loss of visualacuity
Able to sign the consent
Affiliated to the social security system
Already under conventional treatment of Horton's disease or the: requiring:Corticosteroids and + - anti-platelet aggregators and / or LMWH at the discretion ofthe referring physician for its vasculitis and + - immunosuppressive or biotherapy ifnecessary.
Exclusion
Exclusion Criteria:
Underlying hepatocellular insufficiency known
Patient under guardianship or curator
Hypersensitivity to the active substance or to any of the excipients
Moderate to severe hepatic insufficiency corresponding to class B or C of theChild-Pugh classification
Any other ophthalmological pathology explaining the sudden drop in vision: retinaldetachment, retinal hemorrhage, posterior uveitis, nonarteritic arterial occlusion,cortical stroke
Serum levels of hepatic aminotransferases, aspartate aminotransferases (ASTs) and / oralanine aminotransferases (ALATs), greater than 3 times the upper limit of normalbefore start of treatment
Patient under treatment with cyclosporine A, antiretrovirals, glibenclamide orRifampicin.
Pregnant or lactating women
Study Design
Connect with a study center
CH de Cannes
Cannes,
FranceSite Not Available

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