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作 者:邱园华[1] 陈恩国[1] 戴元荣[2] 任振义[3] 周新[4] 施敏骅[5] 蒋汉梁[1] 应可净[1]
机构地区:[1]浙江大学医学院附属邵逸夫医院,杭州310020 [2]温州医学院附属第二医院,浙江温州325027 [3]杭州市第一人民医院,杭州310006 [4]上海市第一人民医院,上海200080 [5]苏州大学附属第二医院,江苏苏州215004
出 处:《中国药学杂志》2012年第21期1760-1763,共4页Chinese Pharmaceutical Journal
摘 要:目的与市售进口品乙酰半胱氨酸注射液(富露施)雾化吸入比较,评价国产吸入用乙酰半胱氨酸溶液祛痰的有效性和安全性。方法本试验采用多中心、随机、双盲、阳性药平行对照设计。选用已经上市的同种进口药物富露施作为对照。共收集急慢性下呼吸道感染患者234例,试验药物组117例,对照组117例。各取3 mL药物,雾化吸入,bid,总疗程5~7 d。统计学上采用非劣效检验及双侧检验。结果试验组的有效率为74.8%(PPS),74.1%(FAS),与对照组比较差异无统计学意义(P>0.05)。在研究过程中,没有发生严重不良事件和重要不良事件。试验组不良事件发生率为14.5%,与对照组比较差异无统计学意义(P>0.05)。根据预设的非劣界值15%,两组非劣效结论成立。结论吸入用乙酰半胱氨酸溶液与富露施比较,祛痰疗效和安全性相当。ABSTRACT : OBJECTIVE To evaluate the clinical efficacy and safety of domestic inhaled N-acetyl-L-cysteine (NAC) solution in mucolytic therapy. METHODS This was a multi-centre, randomized, double blinded and positive parallel trial. Fluimucil, an im- ported drug with the same active ingredient was used as control. Two hundred and thirty-four patients suffering from acute and chronic lower respiratory tract infection were enrolled, 117 patients in study group and control group respectively. Both groups were treated by respective drug 3 mL given by inhalation, bid, for 5 - 7 d. Non-inferiority test and two-sided test were used to analyze the statistic difference. RESULTS The effective rates of the study group were 74. 8% (PPS) and 74. 1% (FAS). There was no significant difference (P 〉 0. 05 ) between the two groups. There were no serious adverse events and major adverse events during the study. The incidence of adverse events in study group was 14. 5%. There was no significant difference (P 〉0. 05 ) between the two groups. Ac- cording to the preset non-inferior creteria, ie 15%, the non-inferiority of the test drug was established. CONCLUSION The clinical efficacy and safety of the domestive inhaled N-acetyl-L-cysteine solution in mucolytic therapy are equal to fluimucil. KEY WORDS : inhaled N-acetyl-L-cysteine solution ; mucolytic therapy ; multi-centre ; clinical trial
关 键 词:吸入用乙酰半胱氨酸溶液 祛痰 多中心 临床试验
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