Primary objective of the study was to evaluate the safety and efficacy of canakinumab on the clinical and inflammatory findings of Behced Disease patients with neurologic and vascular involvement.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of Participants With Attacks
Timeframe: 30 days
Modified Expanded Disability Status Scale (EDSS)
Timeframe: 30 days
Neuro-Behçet's Disability Score (NBDS)
Timeframe: 30 days
Modified Ranking Score (mRS)
Timeframe: 30 days
Ataxia
Timeframe: 30 days
Physical Examination Scores Indicating Change in Muscle Strength
Timeframe: 30 days
C-reactive Protein (CRP) Values
Timeframe: 30 days
Erythrocyte Sedimentation Rate (ESR)
Timeframe: 30 days
SAA (Serum Amyloid A)
Timeframe: 30 days
Hemoptysis
Timeframe: 30 days
Visual Analogue Scores (VAS) for Headache
Timeframe: 30 days
Visual Analogue Scores (VAS) for Stomachache
Timeframe: 30 days
Visual Analogue Scores (VAS) for Extremity Assessments
Timeframe: 30 days
Visual Analogue Scores (VAS) for Patients' General Assessments
Timeframe: 30 days
Physician's Global Assessment
Timeframe: 30 days
Steroid Dose Regimen
Timeframe: 30 days
BDCAF (Behçet's Disease Current Activity Form)
Timeframe: 30 days
Extremity (Localized) Pain Assessment (VAS)
Timeframe: 30 days