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安慰剂

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The scores of neuropsychiatric side effects were lower in neurostan group as compared with placebo group during the treatment.

精神量表评分在治疗组的治疗过程中无明显变化,安慰剂组的量表评分显著高于治疗前和治疗组。

Teriparatide reduced the risk of any new, new adjacent, and new nonadjacent vertebral fractures by 72%, 75%, and 70%, respectively, compared with the rates in the placebo group.

安慰剂组对比,特立帕肽降低新鲜骨折、新鲜邻近椎体骨折、新鲜非邻近椎体骨折发生率分别为72%, 75%, 70%,而雷洛昔芬分别为54%, 54%, and 53%。

Methods: Data from the Fracture Prevention Trial and the Multiple Outcomes of Raloxifene Evaluation trial were analyzed to determine the incidences of new adjacent and new nonadjacent vertebral fractures in the placebo groups and the effect of treatment with raloxifene and teriparatide on the incidence of new adjacent vertebral fractures as compared with that of new nonadjacent vertebral fractures.

研究数据来自于骨折防预试验中心,比较雷洛昔芬与安慰剂组对椎体骨折后再发生邻近椎体骨折及非邻近椎体骨折的发生率以及应用特立帕肽、雷洛昔芬对椎体骨折后再发生邻近椎体骨折及非邻近椎体骨折的风险情况。

Objective: To evaluate the efficacy and safety of Prostat in combination with an antibiotic for the treatment of chronic nonbacterial prostatitis.

舍尼通是一种花粉提取物,已在国内外广泛用于慢性非细菌性前列腺炎的治疗,并取得了一定疗效[1,2],舍尼通与抗生素联合用药是否能更有助于慢性非细菌性前列腺炎临床症状的缓解,尚缺乏多中心、双盲、随机、安慰剂对照的研究报告。

Results: Among the 1699 subjects included in the efficacy analysis, NXY-059 significantly improved the overall distribution of scores on the modified Rankin scale, as compared with placebo (P = 0.038 by the Cochran-Mantel-Haenszel test). The common odds ratio for improvement across all categories of the scale was 1.20 (95 percent confidence interval, 1.01 to 1.42). Mortality and rates of serious and nonserious adverse events were each similar in the two groups.

结果:在1699例可进行有效分析的患者中,NXY-059较安慰剂显著改善了患者改良Rankin量表评分的总体分布(CMH检验P=0.038),量表所有项目的评分都得到改善的共同OR值为1.20(95%CI1.01~1.42),两组患者的死亡率及严重和不严重副作用的发生率均相似。

Main outcome measures The use of 21 classes of prescription medication was compared in the hormone therapy arms and placebo or nontreatment trial arms.

主要结果测量方法:比较该试验激素替代治疗组(2个亚组)、安慰剂组和非治疗组21类处方药的使用情况。

Design Follow up of a randomised controlled trial with a blind subtrial of hormone therapy versus placebo and a nonblind subtrial of open label hormone therapy versus nontreatment.

设计:随机对照试验设计:亚组盲法激素替代治疗 vs安慰剂治疗和亚组非盲法激素替代治疗 vs非治疗,并随访。

Design Follow up of a randomised controlled trial with a blind subtrial of hormone therapy ersus placebo and a nonblind subtrial of open label hormone therapy ersus nontreatment.

设计:随机对照试验设计:亚组盲法激素替代治疗 s安慰剂治疗和亚组非盲法激素替代治疗 s非治疗,并随访。

METHODS: Eighty-eight patients were randomized to receive paravertebral injections with either ropivacaine 0.5%(30 mL) or an equivalent amount of isotonic saline.

88名患者随机在脊柱旁注射0.5%罗哌卡因(30ml )或者等量的等张生理盐水。9名患者被排除出去,剩下79名患者进行评估。(罗哌卡因, n = 38;安慰剂, n = 41。

The median PASI improvement was 46% in etanercept-treated patients versus 9% in placebo-treated patients; similarly, median target lesion improvements were 50% and O, respectively.

治疗12周后, Etanercept组中有26例(87%)达到PsARC,22例(73%)达到ACR20,5例皮损好转75%,而安慰剂组中达到上述标准的分别为7例(23%)、4例(13 %)和0例。

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