Prednisolone in Active Ankylosing Spondylitis (AS)
Ankylosing Spondylitis
About this trial
This is an interventional treatment trial for Ankylosing Spondylitis focused on measuring treatment, ankylosing spondylitis, prednisolone, trial, steroid
Eligibility Criteria
Inclusion Criteria: ankylosing spondylitis according to the modified NY criteria 1984 age between 18 and 70 years insufficient response to therapy with NSAIDs BASDAI > 4 Previous therapy with DMARDs (such as sulfasalazine, methotrexate etc.) or steroids less than or equal to 7,5mg is allowed, should be discontinued or stable 4 weeks before study start written informed consent Exclusion Criteria: Pregnancy or lactation current severe infection or during the last 3 months suspected opportunistic infection during the past 2 months (such as Herpes zoster, cytomegaly-, Pneumocystis carinii-infection), HIV-infection Malignancies severe cardial, renal, hematological, endocrinological, pulmonal, gastrointestinal (such as peptic ulcers) neurological, hepatic (viral or toxic hepatitis) concomitant disease, uncontrolled arterial hypertension remitting thrombosis, embolism Diabetes mellitus or increased blood glucose test uncontrolled glaucoma active immunization during the past 2 weeks or planned for the next 8 weeks pathologic laboratory test results: creatinine >200 µmol/l, liver enzymes > 2,5 fold, AP >2,5 fold upper normal ranges significant pathological changes during physical examination clinical trial participation during the past 30 days before screening intake of "hard drugs" (such as cocaine, heroin) therapy with more than 7,5 mg prednisolone, intraarticular steroids during the past 4 weeks before study start current application for retirement
Sites / Locations
- Charité Campus Benjamin-Franklin RheumatolgyRecruiting
- Immanuel Hospital RheumatologyRecruiting
- Rheumazentrum RuhrgebietRecruiting