This study evaluates the safety of defibrotide with IVIG in children with high risk Kawasaki disease.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2
Defibrotide 6.25 mg/kg IV q6h up to 7 days
Columbia University
New York, New York, United States
New York University
New York, New York, United States
Mitchell Cairo
Valhalla, New York, United States
Number of patients with grade III/IV allergic reaction to defibrotide
All patients will be monitored for allergic reaction probably or definitely related to defibrotide administration.
Time frame: 30 days
Number of patients with grade III/IV hemorrhage attributable to defibrotide
All patients will be monitored for hemorrhage probably or definitely related to defibrotide.
Time frame: 42 days
Number of patients with improvement in clinical progression/signs of Kawasaki disease
Patients will have pre and post treatment assessments with imaging and blood tests to monitor clinical signs of Kawasaki disease
Time frame: 42 days
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