同时，试验组患者较少发生不良反应。
There were less adverse reactions in the experimental group as well.
试验组和对照组各30例。
方法分试验组和对照组。
当然在针对性试验组中，29%志愿者的治疗成功。
Of those in the targeted-trial group, 29% responded positively to the therapy.
而其他两试验组与对照组间突变频率在3%左右。
The frequency of mutation is about 3% between other testing group and comparison of group.
结果：在整个试验组，血管更大并且FMD严重受损。
RESULTS: in the whole examined group, the vessel size was larger and FMD was significantly impaired.
经过四周的治疗，临床和试验组的疼痛均显示明显降低。
Following the four weeks of treatment, both clinical and experimental pain reported were reduced significantly.
试验组添加蛋鸡用复合绿色饲料添加剂，对照组不添加。
The green additive was added in test group hens, while the control group was not.
试验组可能仍然很热所以使用时要小心处理，以免受伤。
Test pack may still be hot so use caution when handling to avoid injury.
试验组睡眠质量改善后，安眠药使用次数也减少了12%。
The yoga group showed these improvements in sleep while simultaneously reducing their use of sleep medication by 12 per cent.
方法：采用数字表随机分组，将护生分为试验组和对照组。
Methods: The students were randomly divided into the experiment group and the control group.
试验组报告生活质量有6%的改善，而对照组则无任何变化。
And the yoga group also reported a 6 per cent improvement in quality of life compared with no change in the control group.
试验组比对照组每只鸡多获利润0.48元，增收效益明显。
The benefit of testing group were 0.48 Yuan higher than it in control group per layer.
在1 ~2周龄时试验组胸腺组织结构出现轻微退化现象。
At 1 ~ 2 week-age, the thymus structure in the experiment group presented a light degeneration.
对照组饲喂基础日粮，试验组在基础日粮中添加1%中药复合剂。
Control group feed basal diet, treatment group add 1%chinese medicine complex among basal diet.
试验组有34例(81.0%)患者对无创通气有较好的依从性。
In trial group 34 (81.0%) patients could tolerate noninvasive ventilation well.
结果66例病人入组并完成试验，试验组33例，对照组33例。
Results 66 patients were enrolled and completed in the study, each group has 33 patients.
结果：试验组临床疗效总有效率达96.92%，与对照组相当。
Results: There were no significant differences between the adjunctive therapy group (with total effective rates being 96.92%) and control group.
随机将大鼠分为正常对照组、假手术组、急性心肌缺血试验组和窒息组。
The rats were randomly divided into normal control group, pseudo surgery group, surgery group and asphyxia group.
试验组在用药后3个月的BI、MMSE评价比用药后1个月时有显著进步。
Evaluation of BI and MMSE was more remarkably improved at 3 month than 1 month in experimental group.
在靶向试验组中，29%的被试验者有着正向反应(四个人的肿瘤完全消失)。
Of those in the targeted-trial group, 29% responded positively to the therapy. (the tumours of four disappeared altogether.)
结果统计分析显示试验组治疗前后血红蛋白、血清铁蛋白、血清铁显著升高。
Results the statistical analysis showed that the hemoglobin, serum ferritin and serum iron improved obviously after treatment.
结果219例患者按方案完成研究，其中试验组114例，安慰剂组105例。
Results 219 patients completed the study according to the protocol, 114 in Metadoxine group and 105 in placebo group.
结果各试验组阳性对照菌的回收率和稀释剂对照组的回收率均达到70%以上。
Results The recovery rates of each positive control and diluent control were higher than 70%.
当仅仅对女性受访者进行调查时，试验组比对照组多37%的可能性患PBC。
When this was investigated among women only, those in the PBC support group were 37% more likely to develop PBC than women in the comparison group.
这些患者的体重都下降了10%，被分成使用瘦素的试验组和使用安慰剂的对照组。
Their weight was reduced by 10% and they were given either replacement leptin or a placebo.
这些患者的体重都下降了10%，被分成使用瘦素的试验组和使用安慰剂的对照组。
Their weight was reduced by 10% and they were given either replacement leptin or a placebo.
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