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新治君治疗呼吸系统感染的随机盲法多中心临床研究

Multicenter clinical study on Xinzhijun for treatment of Respiratory tract infection

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【作者】 阎锡新胡成平刘升明张永祥王廷春李苌清王霆

【Author】 YAN Xixin1,HU Chengping2,LIU Shengming3,ZHANG Yongxiang4,WANG Tingchun5,LI Changqing6,WANG Ting6 1.The Second Hospital of Hebei Medical University,Hebei Province,Shijiazhuang 050005,China;2.Xiangya Hospital of Central South University,Hunan Province,Changsha 410013,China;3.Affiliated Hospital of Ji’nan University,Guangdong Province,Guangzhou 510630,China;4.The First Hospital of Hebei Medical University,Hebei Province,Shijiazhuang 050031,China;5.Guangzhou Boji Clinical Research Center of New Drug,Guangdong Province,Guangzhou 510635,China;6.Xiangbei Welman Pharmaceutical CO.Ltd.,Hunan Province,Changsha 410331,China

【机构】 河北医科大学第二医院中南大学湘雅医院暨南大学附属第一医院河北医科大学第一医院广州博济国家新药临床研究中心湘北威尔曼制药有限公司

【摘要】 目的:以注射用头孢噻肟钠配注射用舒巴坦钠(组合包装)为对照,评价新治君(注射用头孢噻肟钠舒巴坦钠)治疗呼吸系感染的有效性和安全性。方法:采用多中心、随机双盲、平行对照的试验方法,实验组和对照组均采用每次3.0 g,每日2次,疗程均为5~14d的治疗方案。试验组和对照组的临床可评价病例均为60例,细菌学疗效评价例数分别为45和50例。结果:试验组和对照组的临床有效率分别为90.00%和85.00%;细菌清除率分别为95.56%和88.00%;药物不良反应发生率分别为4.76%和1.59%;两组均未出现严重药物不良反应。结论:新治君是治疗呼吸系中、重度感染的安全有效药物。

【Abstract】 Objective: To evaluate the efficacy and safety of Xinzhijun(Cefotaxime Sodium and Sulbactam Sodium for Injection) in treatment of respiratory tract infections compared to Cefotaxime sodium for injection plus Sulbactam sodium for injection combination.Methods: A randomized,double-blind,parallel controlled,multicenter trial was conducted,and the dose of Xinzhijun(experimental group) and Cefotaxime sodium for injection plus Sulbactam sodium for injection combination(control group)was 3.0 g,bid for 5-14 days.The total number of final evaluated subjects was 120.The bacterial evaluated subjects were 45 for experimental group and 50 for control group.Results:Clinical efficacy rate and bacterial eradication rate for experimental group was 90.00% and 95.56%,for control group was 85.00% and 88.00%,respectively.The incidence of adverse reaction including whole clinicalreactions and laboratory abnormalities was 4.76% for experimental group and 3.17% for control group.Serious adverse drug reaction did not occur in two groups.Conclusion:The Xinzhijun had an excellent clinical efficacy and good safety profile in treating patients with moderate to severe degree respiratory tract bacterial infections.

  • 【文献出处】 中国当代医药 ,China Modern Medicine , 编辑部邮箱 ,2011年23期
  • 【分类号】R56
  • 【被引频次】1
  • 【下载频次】103
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