Multicenter, double-blind, multiple-dose, parallel-groups efficacy and safety trial of azelastine, chlorpheniramine, and placebo in the treatment of spring allergic rhinitis
| Autor: | James L. Perhach, John M. Weiler, George R. Hemsworth, Louis Diamond, John T. Connell, Bruce H. Campbell, Richard R. Rosenthal, Lyle H. Hamilton, Arlene Donnelly |
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| Rok vydání: | 1988 |
| Předmět: |
Adult
Male Chlorpheniramine Allergy Evening Adolescent Immunology Placebo Dizziness Drug Administration Schedule law.invention Placebos Double-Blind Method Randomized controlled trial law Statistical significance medicine Humans Multicenter Studies as Topic Immunology and Allergy Chlorpheniramine Maleate Clinical Trials as Topic business.industry Rhinitis Allergic Seasonal Middle Aged Chlorphenamine medicine.disease Azelastine Circadian Rhythm Pyridazines Taste Anesthesia Phthalazines Female Seasons Sleep Stages business medicine.drug |
| Zdroj: | Journal of Allergy and Clinical Immunology. 82:801-811 |
| ISSN: | 0091-6749 |
| DOI: | 10.1016/0091-6749(88)90082-6 |
| Popis: | Azelastine, a novel antiallergic medication, was compared with chlorpheniramine maleate and placebo for efficacy and safety in the treatment of spring allergic rhinitis in a multicenter, double-blind, multiple-dose, parallel-groups study. One hundred fifty-five subjects participated. Subjects ranged in age from 18 to 60 years of age and had at least a 2-year history of spring allergic rhinitis, confirmed by positive skin test to spring aeroallergens. Medications were given four times daily; the azelastine groups received 0.5, 1.0, or 2.0 mg in the morning and evening with placebo in the early and late afternoon; the chlorpheniramine group received 4.0 mg four times daily. Daily subject symptom cards were completed during a screening period to assess pretreatment symptoms and during a 4-week treatment period while subjects received study medications. Individual symptoms, total symptoms, and major symptoms were compared to determine efficacy of medication. Elicited, volunteered, and observed adverse experiences were recorded for each subject and compared among groups. Vital signs, body weights, serum chemistry values, complete blood cell counts, urine studies, and electrocardiograms were obtained for each subject and compared among groups. Symptoms relief in the group receiving the highest concentration of azelastine (2.0 mg twice daily) was statistically greater than in the placebo group during all weeks of the study. Lower doses of azelastine were statistically more effective than placebo only during portions of the first 3 weeks of the study. In contrast, although the chlorpheniramine group did have fewer symptoms than the placebo group during the study, the difference never reached statistical significance during any week of the study. There were no serious side effects in any of the treatment groups. Drowsiness and altered taste perception were increased significantly over placebo only in the high-dose azelastine group. Azelastine appears to be a safe, efficacious medication for seasonal allergic rhinitis. |
| Databáze: | OpenAIRE |
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