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。
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 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；
Methods the clinical trial method was adopted, vein transfusion patients were randomly divided into the study group and the control group.
方法采用临床试验研究方法，将静脉输液病人，随机分组。
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 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。
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。
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。
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。
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。
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）；
Methods With the design of sequential trial, the patients were divided into a treatment group and a control group.
方法：采用序贯试验设计方法分治疗组与对照组。
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。
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。
RESULTS: Local hemostasis trial: There were 6 New Zealand rabbits, 11 experimental data in medication group and 13 experimental data in control group;
结果：局部止血试验：新西兰兔6只，用药组实验数据为11个，对照组实验数据为13个；
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: 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: 165cases of ulcerative colitis were divided into two groups: trial group (compound glycyrrhizin) and control group (sulfasalazine). The clinical effects were compared between two groups.
方法：165例溃疡性结肠炎患者随机分为治疗组和对照组，分别给予复方甘草酸苷和柳氮磺胺吡啶治疗，比较两组的临床疗效。
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。
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: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。
The protective trial proved that there was no significant difference between control group and experimental group though the survival time of mice from experimental group had been prolonged.
动物保护性实验表明，虽然与对照组相比免疫组小鼠存活时间有一定的延长，但差异无显著性。
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 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。
Results the trial was completed in 95% of the patients, 2 patients withdrew in the VASOREL group and 4 patients in the control group; but none for the intolerable therapy.
结果试验总完成率95%，其中治疗组2例、对照组4例脱落，无患者因不耐受药物而脱落。
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）。
Methods A randomized controlled trial, the conventional dose used to guide the control group and low dose group to guide the trial of 20 cases;
方法采用随机对照试验方法，采用常规剂量引导的对照组与采用低剂量引导的试验组各20例；
Methods A randomized controlled trial, the conventional dose used to guide the control group and low dose group to guide the trial of 20 cases;
方法采用随机对照试验方法，采用常规剂量引导的对照组与采用低剂量引导的试验组各20例；
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