Is Levocetirizine Less Sedating Than Cetirizine?
Completed · Phase 4 · Has a placebo group
Conditions studied: Allergic Rhinitis
In brief
The purpose of this study is to determine whether cetirizine (zyrtec), levocetirizine (xyzal), and placebo differ in the degree of sedation they produce and their relief of allergy symptoms.
Key facts
- Study ID
- NCT00826943
- Run by
- Vanderbilt University
- People needed
- 30
- Starts
- 2009-01-01
- Expected to finish
- 2009-05-01
- Last updated by the study team
- 2014-02-20
Who can join
Age: 18 and older, up to 77. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- patients 18 years of age or older
- patients with perennial allergic rhinitis sensitized (positive RAST within the last 3 years or wheal greater than or equal to 3 mm within the last 3 years) to either:
- dust mite
- cat (if they own an indoor cat)
- dog (if they own an indoor dog)
- will allow for sensitization to tree, grass, or weed pollen, cockroach, or mold
- history of reported sedation/somnolence when taking cetirizine
- patient must have taken cetirizine for at least 1 week prior to discontinuing it
- patients must have either tolerated levocetirizine in the past or have never tried levocetirizine.
You may not qualify if…
- chronic urticaria requiring ongoing antihistamine or steroid treatment
- atopic dermatitis requiring ongoing antihistamine or steroid treatment
- URI or sinus infection during the 2 weeks preceding the beginning of the study
- vasomotor (non-allergic) or irritant rhinitis
- afrin use
- elderly or over 77 years of age (could affect creatinine clearance) or chronic renal insufficiency
- patients who have not tolerated levocetirizine in the past due to sedation.
- taking other prescription or over the counter antihistamines and unwilling to stop them during the study
- the presence of a sleep disorder such as sleep apnea or narcolepsy
- the use of as needed sleeping aid medication
- the presence of other chronic medical conditions which in the opinion of the investigator would prevent the subject from being able to participate effectively
Where it is running
- Vanderbilt University Asthma, Sinus, and Allergy Clinic — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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