Chervinsky P, Grossman J, Freitag J J
Allergy and Asthma Center, North Dartmouth, MA 02747, USA.
J Asthma. 1995;32(2):141-5. doi: 10.3109/02770909509083235.
The aim of this double-blind, multicenter trial was to determine the duration of bronchodilating activity of a single 4-mg dose of azelastine in chronic asthmatics. Eligible patients had an FEV1 of 40-79% of predicted value with demonstrated reversibility of airway obstruction. A single dose of azelastine 4 mg resulted in rapid onset of bronchodilating activity with a 12-hr duration of action as demonstrated by a clinically and statistically significant mean percent improvement in FEV1, from hours 2-12. As an overall measure of improvement in FEV1, the area under the curve was statistically significantly greater for azelastine than for placebo. Mean improvements in symptom severity in the azelastine group exceeded those for placebo at all observation points. No serious adverse experiences were associated with azelastine.
这项双盲、多中心试验的目的是确定单剂量4毫克氮卓斯汀对慢性哮喘患者的支气管扩张活性持续时间。符合条件的患者FEV1为预测值的40%-79%,且气道阻塞具有可逆性。单剂量4毫克氮卓斯汀可迅速产生支气管扩张活性,作用持续时间为12小时,这在第2至12小时FEV1的临床和统计学显著平均改善百分比中得到体现。作为FEV1改善的总体衡量指标,氮卓斯汀组曲线下面积在统计学上显著大于安慰剂组。在所有观察点,氮卓斯汀组症状严重程度的平均改善均超过安慰剂组。未发现与氮卓斯汀相关的严重不良事件。