Placebo
DrugSaline, Sub-Cuteanous (SQ)
Other names: Normal Saline
NCT Number: NCT00139152
The purpose of this study is to study the effects of Xolair using non-invasive techniques from the expired gas of patients with moderate to severe allergic asthma.
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Notify Me12 year and older
All sexes
Interventional
Phase 4
Creighton University Division of Allergy & Immunology, Omaha, Nebraska, United States
Traditional methods of sampling secretions from the lower respiratory tract include sputum collection, sputum induction, and bronchoscopy with bronchoalveolar lavage. They cannot be repeated within a short period of time because of their invasiveness, and because the procedures themselves may include an inflammatory response. The need to monitor inflammation in the lungs has led to the exploration of exhaled gases and condensates. Noninvasive monitoring may assist in differential diagnosis of pulmonary diseases, assessment of disease severity and response to treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Saline, Sub-Cuteanous (SQ)
Other names: Normal Saline
Xolair, 0.016 mg/kg Immunoglobulions E (IgE) , SQ
Other names: omalizumab, rhumabE25
Time frame: post dose
Time frame: post dose
Creighton University
Other
Exhaled Breath Condensate and Nitric Oxide: Non-invasive Evaluation of Lung Disease After Treatment With Xolair
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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