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)。
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 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。
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。
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。
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)。
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。
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。
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 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 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。
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。
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;
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。
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。