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randomized double-blind double-dummy
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  随机双盲双模拟
     Bupropion-sustained release in treatment of depression (72 patients) : a randomized, double-blind, double-dummy, multi-center clinical trial
     安非他酮缓释片治疗抑郁症72例的随机双盲双模拟多中心临床研究
短句来源
     Methods A randomized, double-blind,double-dummy, repaglinide-controlled and multicenter clinical trial was conducted. Two hundreds twenty eight patients with type 2 diabetes mellitus were enrolled inthis study, in which 111 patients received nateglinide(trial) and 117 patients receivedrepaglinide(control), for 12 weeks.
     方法 用多中心随机双盲双模拟平行对照的试验设计,观察了228例2型糖尿病病人,其中那格列奈组111例,瑞格列奈组117例。
短句来源
     Baolean Powder in Treatment of 61 Patients with Acute and Chronic Diarrhea:A Randomized Double-blind Double-dummy,Controlled Trial
     宝乐安散剂治疗急慢性腹泻61例随机双盲双模拟对照试验
短句来源
     Compound famotidine chewing tablets relieve gastric acid associated symptoms:a randomized,double-blind,double-dummy,multicenter controlled study
     复方法莫替丁咀嚼片缓解胃酸相关性症状随机双盲双模拟多中心研究
短句来源
     Randomized double - blind double - dummy controlled clinical trial of tiotropium bromide in the treatment of chronic obstructive pulmonary disease
     噻托溴铵治疗慢性阻塞性肺疾病随机双盲双模拟对照临床试验
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  “randomized double-blind double-dummy”译为未确定词的双语例句
     Randomized, double-blind, double-dummy, controlled clinical trial of nateglinide in the treatment of type 2 diabetes
     那格列奈片治疗2型糖尿病的多中心随机双盲平行对照临床试验
短句来源
     Comparison of tiotropium inhalation capsules and ipratropium metered dose inhaler in a randomized,double-blind,double-dummy,efficacy and safety study in patients with chronic obstructive pulmonary disease
     吸入噻托溴铵干粉与异丙托溴铵定量气雾剂治疗慢性阻塞性肺疾病的疗效与安全性比较
短句来源
     Methods A randomized, double - blind, double-dummy , ipratropium - controlled clinical trial was conducted in 44 patients with COPD. Of them, 21 patients were treated by tiotropium (18 μg, qd inhaled ) and 23 patients were treated by ipratropium (40 μg, q6h inhaled) for 4 weeks.
     方法用双盲双模拟随机对照方法,观察了COPD病人吸入噻托溴铵(21例, 18μg,qd)与异丙托溴铵(23例,40μg q 6 h)的支气管扩张作用及安全性。
短句来源
     METHODS To compare with fluoxetine,the randomized,double-blind,double-dummy clinical trial was designed for this study.
     方法采用随机、双盲、双模拟、氟西汀平行对照、多中心临床研究的方法。
短句来源
     Methods The trial was a randomized,double-blind,double-dummy and control design.
     方法多中心(26个中心)、随机、双盲、双模拟的对照研究。
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  相似匹配句对
     DESIGN: Double blinded and randomized design.
     设计随机分组双盲设计。
短句来源
     DESIGN:Randomized and double blind observation.
     设计:随机双盲法观察。
短句来源
     Methods: Randomized double blind study was employed.
     方法:随机双盲对照临床研究。
短句来源
     Methods Prospective, randomized, double-blind study.
     方法 临床试验采用随机、双盲法。
短句来源
     Double blinded randomized controlled trial.
     设计:随机、双盲对照研究。
短句来源
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  randomized double-blind double-dummy
The aim of the study was to assess the relative bioavailability of selenite versus organic Se-yeast in a Se-deficient area in China with a randomized double-blind double-dummy design.
      


Objective:to study the efficacy and safety of moclobemide in comparison with typical antidepressant imipramine Method:200 depressive patients were enrolled for the randomized double blind double-dummy study The dosage of moclobemide was 300-600 mg/d, that of imipramine was 75-250 mg/d Result:at the end of trial, both two groups had lower scores of HAMD and HAMA than before There was no significant difference between the two groups in clinical effect, the effective rate of moclobemide was 79...

Objective:to study the efficacy and safety of moclobemide in comparison with typical antidepressant imipramine Method:200 depressive patients were enrolled for the randomized double blind double-dummy study The dosage of moclobemide was 300-600 mg/d, that of imipramine was 75-250 mg/d Result:at the end of trial, both two groups had lower scores of HAMD and HAMA than before There was no significant difference between the two groups in clinical effect, the effective rate of moclobemide was 79 4%, that of imipramine was 85 4% Moclobemide group had fewer side effects than imipramine group Conclusion:moclobemide is a safe and effective antidepressant

目的 :以经典抗抑郁药物米帕明为阳性对照药采用随机双盲双模拟方法对吗氯贝胺和米帕明治疗抑郁症的疗效和安全性进行研究。方法 :共纳入病人 2 0 0例 ,分别口服吗氯贝胺 3 0 0 -60 0mg d或米帕明75 -2 5 0mg d。结果 :两组病人Hamilton抑郁量表 (HAMD)以及Hamilton焦虑量表 (HAMA)总分在治疗结束时均显著下降 (P <0 0 0 1)。两组之间疗效无显著差异 (p >0 0 5 )。治疗结束时HAMD减分率分别为吗氯贝胺组 0 74± 0 2 4,米帕明组 0 74± 0 2 4(P >0 0 5 ) ;有效率吗氯贝胺组 79 4% ,米帕明组 85 4% (P >0 0 5 )。吗氯贝胺组有 10种不良反应发生频率显著低于米帕明组 ,主要是抗胆碱能、中枢神经系统及心血管系统不良反应。吗氯贝胺的疗效指数也显著高于米帕明组。结论 :吗氯贝胺是一种安全有效的抗抑郁药物

Objective To observe the efficacy and safety of baolean powder (including clostridium butyricum) in treatment of acute and chronic diarrhea.Methods A randomized double-blind double-dummy,multi-center and controlled trials were adopted in the studies.126 patients were divided to receive three times daily baolean powder of 1.0 g(10×108cfu),or three times daily miya tablet of 0.7 g(7.0×108cfu) for 3~7 d or 14~21 d.Results For treatment of acute and chronic diarrhea,the effective rate of baolean powder was...

Objective To observe the efficacy and safety of baolean powder (including clostridium butyricum) in treatment of acute and chronic diarrhea.Methods A randomized double-blind double-dummy,multi-center and controlled trials were adopted in the studies.126 patients were divided to receive three times daily baolean powder of 1.0 g(10×108cfu),or three times daily miya tablet of 0.7 g(7.0×108cfu) for 3~7 d or 14~21 d.Results For treatment of acute and chronic diarrhea,the effective rate of baolean powder was 100.0%(29/29) and 100.0% (32/32) respectively,and miya tablet was 100.0%(32/32) and 100.0%(33/33),respectively.No significant differences (χ 2=0.0,P>0.05) were observed between baolean powder and the control drug (miya tablet) in studies.Conclusion Baolean powder is an effective agent in treatment of acute and chronic diarrhea,the efficacy and safety of baolean powder are similar to those of miya tablet.

目的观察宝乐安散剂治疗急慢性腹泻的临床疗效和安全性。方法采用多中心随机双盲、双模拟对照试验。宝乐安散剂61例,po,1.0g(10×108cfu),tid;对照药米雅片65例,po,0.7g(7.0×108cfu),tid。疗程急性腹泻3~7d,慢性腹泻14~21d。结果宝乐安散剂治疗急性腹泻有效率为100.0%(29/29),慢性腹泻有效率为100.0%(32/32);对照药米雅片分别为100.0%(32/32)和100.0%(33/33)。两药疗效间差异均无显著性(χ2=0.0,P>0.05),均未出现不良反应。结论宝乐安散剂是治疗急性、慢性腹泻安全有效的微生态制剂,其疗效和安全性均相当于进口药米雅片。

 
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