Xolair in Patients With Chronic Sinusitis
Sinusitis
About this trial
This is an interventional treatment trial for Sinusitis focused on measuring chronic sinusitis
Eligibility Criteria
Inclusion Criteria: Chronic sinusitis, as defined by symptoms for greater than 12 weeks, despite treatment Paranasal sinus CT scan showing evidence of chronic sinusitis Positive skin or RAST test to an inhalant allergen Serum total IgE between 30 and 700 International Units/ml Body weight less than 150 kg Impaired quality of life, as measured by the Rhinosinusitis Disability Index (RSDI) Exclusion Criteria: Women of childbearing potential not using a contraception method(s) (birth control pills, Depo Provera, double barrier) as well as women who are breastfeeding Known sensitivity to Xolair Patients with severe medical condition(s) that, in the opinion of the investigator, prohibits participation in the study (heart, lung, kidney, neurological, oncologic or liver disease) Use of any other investigational agent in the last 30 days No measurable disability on the RSDI Immunocompromised patients or patients with ciliary disorders
Sites / Locations
- The University of Chicago
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
1
2
Xolair administered subcutaneously, once or twice monthly (dose dependent on subject weight and serum IgE level)
placebo administered subcutaneously once or twice monthly