The authors note that neurocognitive test performance over the duration of treatment was comparable to that of a matched group of controls.
作者注意到在治疗过程中神经认知测试表现，实验组比得上对照控制组。
Impressively, the learning of the second group also was comparable to that of a third group that for a week practiced the pitch-discrimination target task for 40 minutes per day.
第二组的学习成果与第三组相似，而第三组是连续一星期每天训练40分钟，这非常令人震惊。
Standard propensity score matching was used to create a highly comparable control group.
标准倾向评分匹配(Standard propensity score matching)用来创建一个高度可比的对照组。
Patients are divided into a winning group and a comparable losing one on the basis of therapeutic efficacy.
按治疗效果将病人划分为成功组与可比的失败组，就试药服用比例在两组间进行比较。
ResultsBaseline of the experimental group and control group showed no difference (P> 0.05), between the two groups were comparable.
结果基线时实验组和对照组各项指标无差异（P>0.05），说明两组间具有可比性。
In each company, 2 comparable work units were randomly allocated, resulting in 18 clusters with 258 workers assigned to the intervention group and 231 workers to the control group.
在每个公司中，随机组成了2人单位，总共有18个群体，其中258人为介入组，另外231人为对照组。
RESULTS: YTT group was comparable with control group in general conditions. The effective rates of both groups were 100% without ADRs.
结果：随机对照的两组患者一般情况可比，两组有效率均为100％，均未发现不良反应；
Meanwhile the clinical symptoms in thalidomide group improved faster, and the improvement of liver function was comparable with control group.
沙利度胺组临床症状改善较快，退黄时间和转氨酶下降速度与对照组相近。
ResultsPatients into 2 groups when the baseline group difference was not statistically significant, comparable.
结果两组患者入组时的基线情况差异无统计学意义，具有可比性。
ResultsCompare with gender, age composition and lesion side and severity of?he treatment group and control group, the diagnostic standards have no statistical significance (P>0.05). It is comparable.
结果治疗组与对照组患者的性别、年龄构成及患侧、病情轻重等指标经过统计学检验，无明显差异（P>0.05），具有可比性。
ResultsCompare with gender, age composition and lesion side and severity of?he treatment group and control group, the diagnostic standards have no statistical significance (P>0.05). It is comparable.
结果治疗组与对照组患者的性别、年龄构成及患侧、病情轻重等指标经过统计学检验，无明显差异（P>0.05），具有可比性。
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