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机构地区:[1]兰州军区兰州总医院药物临床试验机构,甘肃兰州730050
出 处:《西北国防医学杂志》2012年第6期630-633,共4页Medical Journal of National Defending Forces in Northwest China
摘 要:目的:评价注射用阿莫西林克拉维酸钾颗粒(8∶1)治疗急性呼吸道感染的有效性和安全性。方法:采用多中心、随机、双盲、平行对照试验设计,共入选病例136例,其中试验组[阿莫西林克拉维酸钾颗粒(8∶1)]69例;对照组[阿莫西林克拉维酸钾片(7∶1)]69例;一般疗程均为7~14 d,最短疗程不少于5 d。结果:试验组治疗有效病例69例,治愈59例,临床痊愈率为89.39%;对照组治疗有效病例69例,治愈61例,临床治愈率为92.42%。细菌清除率:试验组为95.45%,对照组为92.91%,药物不良反应发生率均为4.35%。结论:阿莫西林克拉维酸钾颗粒(8∶1)治疗各种敏感菌所引起的呼吸道感染,安全、有效,使用方便,耐受性好。Objective:To evaluate the efficacy and safety of amoxicillin and clavulanate potassium granules(8∶1) in the treatment of acute infection of respiratory system.Methods: A multicenter,randomized,double-blind,controlled clinical trial was conducted in the treatment of 138 patients with acute infection of respiratory system.There were 69 cases in the trial group:amoxicillin and clavulanate potassium granules(8∶1),while 65 cases were in the control group:amoxicillin and clavulanate potassium gispersible tablets(7∶1).The treatment duration for both groups was from 7 to 14 days(at least 5 days).Results: The effective rate for the trial and control group was 89.39% and 92.42% respectively.The bacterial eradication rate was 95.45% and 92.91% respectively.The incidence of adverse reactions was 4.35% in both groups.Conclusion: Amoxicillin and clavulanate potassium granules(8∶1) is effective and safe in the treatment of acute infectin of respiratory system.
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