Methods 60 patients with malignant pleural effusion were randomly divided into trial group and control group and each group was 30 patients .

方法将60例恶性胸腔积液患者随机分为 观察 组和对照组（各30例）。

After 4 weeks the laying rates of the trial group and control group were 71.99 % and 69.96 % respectively ;

结果表明：用药后4周， 试验 组和对照组的产蛋率分别为71.99%和69.96%；

The enteric epithelial cell of the trial group was integrity and the villi of the intestines developed well .

病理切片观察发现，免疫器官的发育总体上试验 组好于 对照 组； 试验 组肠道上皮细胞完整，肠绒毛发育良好。

Group . CR in the trial group were superior to that in control .

治疗结束时的CR率 试验 组明显高于对照组。

Methods : 240 cases of inpatients of hypertension were randomly divided into a trial group and a control group establishing database and descriptive analysis t-test x ~ 2 test and rank test methods were adopted .

方法：采用临床单纯随机分组方法，将240例住院高血压患者随机分为 试验 组和对照组，建立数据库，运用描述性分析、l检验、X~2检验及秩和检验等方法。

The trial group were treated with asiaticoside injection every week for three months consecutively .

设积雪甙注射剂组为 试验 组，应用积雪甙注射剂瘢痕内注射，每周一次，连续应用3月。

There were still undue diagnoses of different degrees among pathologists of the trial group .

试验 组医师仍存在不同程度的过度诊断。

Trial group ⅱ was improved ( 15.80 % ) on average daily gain 19.51 % on feed efficiency ;

试验Ⅱ 组的日增重提高15.80%，饲料报酬提高19.51%；

The adverse reaction rates of trial group controlled group and open group were 8.47 % 8.93 % and 5.77 % respectively .

随机 对照两组和开放组的不良反应率分别为8.47%、8.93%和5.77%。

20 healthy adult female SD rats 300g-weight were randomly divided into trial group and control group .

健康成年雌性SD大鼠20只，体重约300g，分成 实验 组和对照组，每组10只。

Trial group wore dental stent during radiotherapy while control group did not .

两组患者均采用CT模拟常规设野的放射治疗技术，在放疗过程中， 试验 组 患者佩戴口腔支架，对照组不佩戴。

RESULTS : Dosimetric analysis proved that the irradiation dose and volume of the tongue decreased obviously in trial group .

结果：剂量学分析表明 患者佩戴口腔支架后舌的受照射剂量和体积均较 佩戴前明显下降。

Results 121 cases in trial group and 63 cases in control group bleeding time were less 14 days .

阴道流血时间小于14天者实验 组121例， 对照 组63例。

In this test 20000-old-day new ROMAN layers were randomly divided into trial group and control on average .

本试验选用0日龄新罗曼商品代蛋鸡2000只，随机分成两组，每组1000只，包括 试验 组和对照组。

This trial group is composed of one judge four judge assistants and two clerks .

这一 审判 组织由1名独任法官，4名法官助理和2名书记员组成。

The results showed that total amounts used the drug for everyone in Beth proups were not significantly different but the accident of the drug side-effects and the amounts taken gastroenteric drug in control group were more than that in trial group .

结果显示：用迪化精锭1－2周后两组日平均用药总量无显著差异，但对照组胃肠道副作用发生率、并用胃肠药物的量均显著高于 试验 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。

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。

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。

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。

Trial group respiration support time is shorter than that of control group ( P < 0.05 ) .

试验 组的术后呼吸支持时间明显少于对照组（P<0.05）；

Compared with the control group the mark in the trial group was obviously improved ( P0.01 ) .

实验组 生理学考核成绩均明显高于 对照 组（P〈0.01）。

Results Morphological observations revealed that the proliferation of fibroblasts in trial group was enhanced and the phenotype modulated by bile .

结果形态学观察显示 胆汁促进成纤维细胞增殖和表型转化。

The development potential of control group is prior to that of the either trial group .

对照组的发展潜能要显著优于 试验 组；

Regular nursing process was conducted both in trial group and control group while in the trial group simultaneously achieved health education .

两 组患者同时接受常规护理， 试验 组在此基础上接受健康教育。

Results The overall patients 90 cases trial group 58 cases controls 32 cases .

结果共治疗病人90例，其中 试验 组58例，对照组32例。

Two Groups after the intervention of Syndrome is Integral Statistically Significant Low Trial Group .

两组干预后的证候积分比较，有统计学差异， 试验 组偏低。

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。