Study of Bronchodilation Effects of Cetirizine
Completed · Phase 4 · Has a placebo group
Conditions studied: Allergic Rhinitis, Asthma
In brief
Primary Objective : To compare the acute bronchodilatory effects of cetirizine 10 mg tablet and nebulized levalbuterol using impulse oscillometry technique in asthmatic subjects aged 18 to 65 years old who have allergic rhinitis and show clinical evidence of bronchial hyper-reactivity. Secondary Objective: To assess the bronchodilatory effects of cetirizine 10 mg tablet versus placebo after two weeks of therapy using impulse oscillometry technique in subjects 18 to 65 years old who have allergic rhinitis and show clinical evidence of bronchial hyper-reactivity.
Key facts
- Study ID
- NCT01781507
- Run by
- California Allergy and Asthma Medical Group, Inc.
- People needed
- 21
- Starts
- 2011-06-01
- Expected to finish
- 2011-12-01
- Last updated by the study team
- 2013-09-04
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age between 18 to 65 years of age
- Physician diagnosis of mild asthma based on the NIH guidelines
- Physician diagnosis of allergic rhinitis and confirmed by at least 3+ skin test response to at least one allergen
- Evidence of abnormal, reversible airway function on impulse oscillometry
- Ability to cooperate in measurement of impulse oscillometry
You may not qualify if…
- Treatment with inhaled or oral corticosteroids within one month of screening visit
- Change in dosage of intranasal corticosteroids, or oral anti- leukotrienes within one month of screening visit. Subjects on constant dose of intranasal corticosteroids or anti-leukotrienes for one month or more will be allowed in the study.
- Known history of reflux, lung disease, or congenital heart disease
- Known history of adverse reaction to cetirizine
Where it is running
- California Allergy and Asthma Medical Group — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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