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安慰剂

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The approval was based on data from four double-blind, randomized trials that compared the antianginal and anti-ischemic efficacy of ivabradine with placebo, atenolol, and amlodipine in 3,222 patients. Results obtained using a standardized exercise tolerance test showed that twice-daily administration of ivabradine, 5 and 7.5 mg, significantly decreased the incidence of anginal episodes.

这项核准案是根据4项双盲随机分派试验结果,这些试验针对3,222位病患,比较Ivabradine相较於安慰剂、atenolol、及amlodipine治疗心绞痛与减少心肌缺血的效果;以标准运动耐受性测试所得到的结果显示,每天投予2次5或是7.5毫客的Ivabradine可以显著地降低心绞痛发生的次数。

There was no change in the anthropometric parameters at the start and end of hGH/placebo therapy.

安慰剂组生长激素的人体测量参数在开始和结束没有变化。

Patients were randomly assigned either dexamethasone (n=24) or placebo (n=19) and receied 9 months of treatment with standard first-line antituberculosis drugs.

患者被随机分成两组,一组给予地塞米松(n=24),一组给予安慰剂(n=19),同时接受9个月的一线标准抗结核药治疗。

Results: At 12 months, aBMD gain was greater at the FDia and at the mean of the fie appendicular skeletal sites in the calcium supplement group in both intention-to-treat analysis 76 ± 32 s.

结果:12个月后,补钙组股骨骨干和五个四肢骨骼位点平均面积骨矿物质密度较安慰剂组显著增加,意愿治疗分析结果显示,股骨骨干面积骨矿物质密度76 ± 32 s。

Results: At 12 months, aBMD gain was greater at the FDia and at the mean of the five appendicular skeletal sites in the calcium supplement group in both intention-to-treat analysis 76 ± 32 vs.

结果:12个月后,补钙组股骨骨干和五个四肢骨骼位点平均面积骨矿物质密度较安慰剂组显著增加,意愿治疗分析结果显示,股骨骨干面积骨矿物质密度76 ± 32 vs。

Schedel et al. investigated the efficacy of Hirudoid forte in 40 patients with postoperI bitis under double-blind conditions in comparison to placebo.

Schedel等人研究了特强喜疗妥软膏的疗效,以安慰剂为对照,双盲,受试对象为40位患者。

Study drug and placebo were provided by Cephalon Inc.

研究药物与安慰剂由Cephalon公司提供。

In a preliminary trial, supplementation with 500 mg of a concentrated extract (3.5% guggulsterones) of Commiphora mukul three times per day for one month resulted in a significant improvement in symptoms in people with OA of the knee.

在初步试验中,补充了500提取集中在与人民的膝关节炎的症状显着改善的结果(3.5%guggulsterones 穆库尔的没药,每日3次)一个月毫克。111双盲试验需要排除安慰剂效应的可能性。

Based on pre-specified intent-to-treat and completer analyses, obese patients treated with Contrave lost an average of 20.3 pounds to 25.0 pounds, or 9.3% to 11.5% of their baseline body weight, versus 11.0 pounds to 16.0 pounds, or 5.1% to 7.3% of baseline body weight, for patients treated with placebo.

根据预先指定的意图治疗和补足分析,肥胖患者失去治疗Contrave平均二十〇点三磅以二十五点○英镑,或9.3 %, 11.5 %的基线体重,与一十一点〇英镑以十六点○磅,或5.1 %至7.3 %的基线体重,对治疗的患者服用安慰剂

The news reports says those received medision did improve .but conferrable numbers who receives both also improved.

新的报告说服用药物的患者症状有所改善。但是服用安慰剂的患者症状也有所改善。

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然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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