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a randomized double-blind
相关语句
  随机双盲
     Impact of zinc supplementation on mental and psychomotor scores of children aged 12 to 18 months: A randomized, double- blind trial
     补锌对12~18月龄儿童智力和精神运动评分的影响:一个随机双盲试验
短句来源
     A Randomized Double-blind Control Clinical Study on Moxifloxacin for Treatment of Bacterial Skin Infections
     莫西沙星治疗皮肤细菌感染随机双盲对照临床研究
短句来源
     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
     Efficacy and safety of adefovir for treating HBeAg positive chronic hepatitis B: A randomized double-blind and controlled trials
     阿德福韦治疗HBeAg阳性慢性乙型肝炎的疗效与安全性——随机双盲对照研究
短句来源
     Methods A randomized,double-blind positive controlled trial was adopted.
     方法70例受试者,采用随机双盲、阳性药平行对照方法,试验组52例,服用龙香平喘胶囊;
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  “a randomized double-blind”译为未确定词的双语例句
     A randomized, double- blind, placebo- cont- rolled trial of the combined effect of doxycycline hyclate 20- mg tablets and metronidazole 0.75% topical lotion in the treatment of rosacea
     20mg多西环素片剂联合局部外用0.75%甲硝唑洗剂治疗酒渣鼻疗效的随机、双盲、安慰剂对照试验
短句来源
     A randomized,double-blind,parallel grouping trial was conducted. Results TSS of test group improved was decreased from 15.67±2.28 to 3.25±3.90,improving rat was(79.90±24.21)%,TSS of control group improved was decreased from 14.71±2.90 to 3.38±2.62,improving rat was(76.44±19.40)%.
     结果治疗1周,试验组靶皮损总积分(TSS)由治疗前15.67±2.28降至3.25±3.90,症状体征改善率为(79.90±24.21)%; 对照组总积分由治疗前14.71±2.90降至3.38±2.62,改善率为(76.44±19.40)%。
短句来源
     Methods: Fourty-six NHL patients were enrolled in a randomized, double-blind, placebo-controlled trial: CHOP plus rh-TNFα-DK2 group (trial group) and CHOP plus placebo group (control group) for 2 cycles.
     方法:对46例NHL患者进行随机、双盲、对照的临床研究,分别以CHOP方案+rh-TNFα-DK2(试验组)和CHOP方案+安慰剂(对照组)化疗2个疗程。
短句来源
     Methods: In a randomized,double-blind and comparative-controlled study,200 patients with major depression (ICD-10 criteria) were randomized to receive imipramine (75-250mg·d-1) or moclobemide(300-600mg·d-1)for a 6-week course of therapy.
     方法:采用双盲对照研究方法将200例符合ICD-10抑郁障碍诊断标准的住院或门诊患者,随机分组接受吗氯贝胺(300-600mg·d-1)或丙咪嗪(75-250mg·d-1)治疗6周。
短句来源
     Methods A randomized,double-blind study was carried out in 68 patients with serious bladder spasm patients received either tolterodine (2mg twice daily)or isoptin (80mg twice daily).
     方法 采用随机、双盲的方法对68例膀胱痉挛频繁发作病人进行托特罗定与异搏停的对比研究,服药方法每日2次,每次托特罗定2mg或异搏停80mg。
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  相似匹配句对
     Methods: A randomized and double blind way performed.
     方法:采取随机双盲对照观察法。
短句来源
     The study was done as a randomized,double-blind trial.
     用随机抽样,双盲法进行实验。
短句来源
     Methods A randomized, double blind study was performed.
     方法 采用随机、双盲研究方法。
短句来源
     Methods:A randomized, double-blind, placebo add-on was taken.
     方法 :随机双盲 ,添加治疗安慰剂对照临床试验。
短句来源
     Methods This was a randomized double - blind comparative study.
     方法 与双益平片剂为对照药,采用多中心前瞻性随机双育方法;
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  a randomized double-blind
A randomized double-blind, parallel group study in 110 patients showed equivalence in efficacy of 900 mg dexibuprofen (Seractil 300 mg, Gebro Fieberbrunn, Austria) vs.
      
Intravenous immune globulin (IVIG), 400 mg/kg daily for 3 days, was administered in a randomized double-blind placebo-controlled trial.
      
A Randomized Double-Blind Study to Compare the Effectiveness of Three Different Doses of Lignocaine Used in Paracervical Block D
      
Future research should also emphasize employing a randomized double-blind placebo-controlled crossover design, as well as involving multicenters and using uniformed diagnostic criteria to study autistic adolescents and adults.
      
The aim was to evaluate the effect of α-galactosidase administration, in a randomized double-blind placebo-controlled protocol, on intestinal gas production and gas-related symptoms after a challenge test meal in healthy volunteers.
      
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A randomized double-blind trial compared brufen (600mgtid) produced in China with that made in England. A total of 31 cases ofdefinite rheumatoid arthritis were involved. Signs and symptoms of thediseases were observed during and after 5 weeks of treatment. Both durgs showed similar abilites to decrease the number of jointsafected by pain and swelling and to improve morning stiffness, withstatistical significance in both cases, No improverment in 20M meterwalking time or grip strength of both hands was...

A randomized double-blind trial compared brufen (600mgtid) produced in China with that made in England. A total of 31 cases ofdefinite rheumatoid arthritis were involved. Signs and symptoms of thediseases were observed during and after 5 weeks of treatment. Both durgs showed similar abilites to decrease the number of jointsafected by pain and swelling and to improve morning stiffness, withstatistical significance in both cases, No improverment in 20M meterwalking time or grip strength of both hands was seen. Four cases of mild side-effects were reported in China's brufen studygroup, but England's brufen had 1 case of anasarca and menorrheanecessitating discontinuation of treatment.

对31例诊断明确的类风湿关节炎病人应用国产及英国产布洛芬1800mg/d,进行了随意抽样双盲试验,观察了在5周的治疗过程中及治疗后有关疾病的症状和体征的改善情况。两种药物对减轻关节的疼痛感、肿胀及晨僵显示了有统计学意义的相近的能力;而对20米步行时间及双手握力也显示了相近的无统计学意义的改善能力。国产布洛芬治疗组有4例发生轻微副作用:1例皮疹未经处理自行消失,3例上腹部不适加用对症药后缓解;英国产布洛芬治疗组有1例用药后5周因面部及周身浮肿、月经增多而被迫停药;另2例分别发生胃部不适及外耳肿痛,前者自行缓解,后者减药后症状消失。

215 cases of chronic cervicitis were treated with low concentration interferon prepared from human umbilical cord blood by spray on the focus of the disease. A randomized double-blind and placebo-eontrolled trial was used in this study. The results obtained from the clinical study showed that the total effective rate of the treated-IFN group was 93.02% (200/215) and the markedly improved rate was 49.77% (107/215). There was very significant difference between the study group and the placebo-controlled...

215 cases of chronic cervicitis were treated with low concentration interferon prepared from human umbilical cord blood by spray on the focus of the disease. A randomized double-blind and placebo-eontrolled trial was used in this study. The results obtained from the clinical study showed that the total effective rate of the treated-IFN group was 93.02% (200/215) and the markedly improved rate was 49.77% (107/215). There was very significant difference between the study group and the placebo-controlled group. It is indicated that the degree and type of chronic cervicitis is related to the therapeutic effect The erosion degree of cervix is slighter, it is easier for the treatment Chronic cervicitis is divided into three types. Among them, the simple type of chronic cervicitis is easily cured and its markedly improved rate was 67.57% (50/74). The second is particle type (51.25%, 41/80). The most difficult for treatment is papillar type (26.23%, 16/61). Moreover, the mechanism of treatment of chronic cervidtis with inteiferon is also discussed

作者应用小剂量人脐血白细胞干扰素以随机双盲对照法对宫颈表面直接喷雾试治慢性宫颈糜烂215例,总有效率达93.02%,显效率以上达49.77%,与对照组相比有非常明显差异。根据作者的研究结果表明,宫颈糜烂的程度和类型与疗效有关。糜烂程度轻则治愈率高;三种类型的宫颈炎,以单纯型较易治,其显效率以上可达67.57%,其次是颗粒型(51.25%),最难治的是乳头型(26.23%)。此外,本文还讨论了干扰素治疗慢性宫颈炎的机制问题。

In a randomized double-blind therapeutic trial, diltiazem or verapamil was given to 53 patients with essential hypertension for 4 wk. Twenty-seven patients (M20,F 7;age 50+7 yr; duration of hypertension 14+7 yr)received maximal diltiazem 270 mg/d,and 26 patients(M 25,F 1;age 52+6 yr; duration of hypertension 14+8 yr) received maximal verapamil 360 mg/d.In diltiazem group,the response rate was 85%, while in verapamil group 46%(P>0.05).The blood pressure in the former was reduced more definitely than that...

In a randomized double-blind therapeutic trial, diltiazem or verapamil was given to 53 patients with essential hypertension for 4 wk. Twenty-seven patients (M20,F 7;age 50+7 yr; duration of hypertension 14+7 yr)received maximal diltiazem 270 mg/d,and 26 patients(M 25,F 1;age 52+6 yr; duration of hypertension 14+8 yr) received maximal verapamil 360 mg/d.In diltiazem group,the response rate was 85%, while in verapamil group 46%(P>0.05).The blood pressure in the former was reduced more definitely than that in the latter(2.0/2.0 vs 1.0/1.0 kPa,P<0.01,P<0.05). The serum HDL-ch was increased without significance in both groups. No serious adverse effects were noticed with both agents.

本文用随机双盲组间对照的方法,对53例原发性高血压进行治疗对比.地尔硫组27例(男20例,女7例;年龄50±SD7yr;病程14±7yr),用最大剂量270mg/d,4wk为一疗程。维拉帕米组26例(男25例,女1例;年龄52±6yr病程14±8yr)用最大剂量360mg/d,4wk为一疗程。总有效率前者大于后者(85%,46%)但差异不显著,降压幅度亦是前者大(2.0/2.0kPa,1.0/1.0kPa,P<0.01,0.05)2药均有升高HDL-ch的作用,副作用均较轻.

 
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