Trial group was more effective, with obvious lower death rate.
治疗组优于对照组，病死率亦明显低于对照组。
Of those in the targeted-trial group, 29% responded positively to the therapy.
当然在针对性试验组中，29%志愿者的治疗成功。
METHODS:60cases of AD were randomly divided into trial group and control group.
方法：60例AD患儿随机分为治疗组和对照组。
In trial group 34 (81.0%) patients could tolerate noninvasive ventilation well.
试验组有34例(81.0%)患者对无创通气有较好的依从性。
Experimental procedure of control group was the same of trial group except being shot.
对照组动物除不枪击外，实验步骤同实验组。
Methods 120 cases of senile osteoporosis were randomly divided into trial group and control group.
方法选择120例老年性骨质疏松症患者，随机分为观察组和对照组。
Methods 72 SD rats were divided into three groups randomly. (empty group, control group and trial group).
方法SD大鼠72只，随机分为治疗组、对照组及空白组。
Methods 72 patients with severe hepatitis were randomly divided into the trial group and the control group.
方法将72例重型肝炎患者随机分为治疗组和对照组，比较两组的临床疗效。
METHODS: 126patients with severe hepatitis were randomly divided into the trial group and the control group.
方法：126例重型肝炎患者随机分为治疗组和对照组，比较两组的临床疗效。
Methods A total of 106 DCM patients with heart failure were allotted into trial group and control group at random.
方法将106例患者随机分为两组，在常规抗心力衰竭基础上，渝疗组加用二丁酰环磷腺苷钙静脉给药；
The average daily milk production capacities of the trial group fed on diet with kelp meal and the control group were 18.
奶牛日粮中添加海带粉的试验组，与不添加的对照组，两组奶牛日均产乳量分别为18。
The above result show that therapy of two groups both can help COPD, and the trial group is better than the control group.
说明两组治疗均可以改善患者症状，且治疗组疗效优于对照组。
Of those in the targeted-trial group, 29% responded positively to the therapy. (the tumours of four disappeared altogether.)
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)。
Results: the total number of all the subjects was 26, including 13 subjects in trial group and 13 subjects in control group.
结果：共入组手足皲裂患者26例，包括试验组和对照组各13例。
The results showed that there was no significant difference on dry matter intake between control group and trial group(P>0.05).
结果表明：试验组和对照组犊牛干物质采食量差异不显著（P>0.05）；
RESULTS: The improvement of scale and total clinical score of trial group for tinea pedis were superior to control group (P<0.01) at 4 weeks;
结果：试验组对足癣，在第4周时脱屑症状的改善和临床的综合改善明显优于对照组（P<0.01）；
The improvement of itching and total clinical score of trial group for tinea corporis & cruris were superior to control group (P<0.05) at 1 weeks;
试验组对体股癣，在第1周时瘙痒症状的改善和临床的综合改善优于对照组（P<0.05）；
The traditional method for continuing education was given in the control group while eligibility - based training model was taken in the trial group.
对照组采用传统的社区卫生服务机构医生继续教育培训方法，试验组采用以胜任为基础的培训模式进行培训。
RESULTS:Roentgenographic scores and callus density at bone defects in trial group were better than those in control group at postoperative 3,6,12weeks.
结果：实验组骨缺损放射影像学评分以及新生骨痂的密度在3，6，12周均优于对照组。
The control group was fed with the basal diets and the trial group was fed with the corn grain of the same quantity instead of corn in the basal diets.
对照组饲喂基础日粮，试验组每以等量整粒玉米替代基础日粮中的玉米。
The digestibility of dry matter and organic matter in trial group were obviously higher than the control group, respectively 8.22 and 5.92 percents higher.
干物质和有机物质的消化率试验组明显高于对照组，分别比对照组提高8.22和5.92个百分点。
The concentration of SOD decreased after operation in both groups(P<0.05), and it was higher in the trial group than the control group at different time points.
两组术后血清SOD含量均低于术前，试验组各时点的SOD均明显高于对照组（P<0.05），试验组下降的程度较对照组明显更小。
RESULTS: Totally 47 patients finished the trial, 23 in the trial group, among which 1 was not accordant with the inclusion criteria, and 24 in the control group.
结果：共有47例完成了试验，其中喷昔洛韦组23例，1例不符合纳入标准。阿昔洛韦组24例。
There was significant difference in clinical symptoms and NIH-CPSI between pre-treatment and post-treatment in the trial group and the control group (P<0.05, P<0.01).
治疗组和对照组临床症状评分、NIH-CPSI评分比较，差异均有统计学意义（P<0.05，P<0.01）。
Results:The results of exam showed that the students in trial group had a significant higher score in sum score and analysis subjects than those in control group(P<0.05).
结果：理论考核成绩表明，实验组在总分及分析综合题得分上明显高于对照组（P<0。05）。教学评估结果也显示：实验组学生学习更主动、更善于独立思考和沟通。但二者并非完全一致。
Results It was more prominent of decrease icterus index, increase seralbumin, the activity of prothrombin and the effective rate in the trial group than in the control group.
结果治疗组在降酶、退黄，提高血清白蛋白、升高凝血酶原活动度，以及治疗有效率等方面均优于对照组，差异具有显著性。
The rates of abnormal results of laboratory test were 0.00% in trial group and 2.08% in control group. There were no significant differences between two groups in safety(P>0.05).
塞克硝唑片组实验室检查异常发生率为0.00%，替硝唑片组实验室检查异常发生率为2.08%，两组之间比较差异无统计学意义（P>0.05）。
Methods PBL teaching was practiced in trial group, while LBL teaching was practiced in control group. The writers made an analysis of this teaching by way of questionnaire and exam.
方法实验组采用PBL教学，对照组采用传统教学，通过理论考试和问卷调查分析教学效果。
But they provide no information for populations with different characteristics from the trial group, such as age, gender, state of health, co-treatment with other medicines and ethnic origin.
但是它们不能提供有关试验组中具有不同特征的人群的信息，诸如年龄、性别、健康状况、与其它药物联合治疗情况以及种族出身。
But they provide no information for populations with different characteristics from the trial group, such as age, gender, state of health, co-treatment with other medicines and ethnic origin.
但是它们不能提供有关试验组中具有不同特征的人群的信息，诸如年龄、性别、健康状况、与其它药物联合治疗情况以及种族出身。
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