trial group

  • trial group
  • 释义

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纠错 数据更新时间:2026-04-19 14:16:02
1、

The clinical effective rate for tinea corporis& cruris at week 4 was 98.21 in the trial group and 92.73 in control group; and 100 versus 98.18 at week 6 respectively.

体、股癣在4周时,临床有效率试验组98.21%,对照组92.73%,在6周时分别为100%和98.18%;

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2、

The increase amounts of body height, chest deep, canno round, rump length, hip bone wide and sciatic wide in trial group were the same as those in control group;

试验组牛体高、胸深、管围、尻长、腰角宽和坐骨端宽的增长量与对照组数据相比,无明显差异(P>0.05);

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3、

Jury, translating problem, trial by peers, decide together, select randomly, group of judge.

陪审; 翻译问题; 同辈审理; 集体决定;随机遴选;裁判团.

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4、

In the paper the main technical features and parameters of EBH/ J-132 roadheader are detailed and its trial production in Wuyang Mine of Lu'an Coal Mining Group is introduced.

本文介绍了EBH/J-132型掘进机的主要技术特点和参数,及其在潞安矿业集团五阳矿试验的情况;

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5、

Safflower yellow pigment lyophilized dripping solution ( SYPLDS) 200 ml ( 160 mg), intravenously guttae, daily ( trial group 3);

试验组3纳入112例,采用红花黄色素滴注液200ml(160mg)静滴,每日1次;

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6、

In the trial group, Patients were given to simiao powder, plus Etanercept with adequate dosage and duration.

试验组给予四妙散加减方联合足量足疗程依那西普治疗,对照组则单纯给予足量足疗程依那西普治疗。

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7、

Results The symptoms of the subjects in trial group such as headache, dizziness, chest distress, dysphoria, tidal fever with perspiration, vaginal discomfort, pudendal dryness and pain, myospasm, arthralgia, etc were alleviated obviously.

结果治疗组患者服用牡蛎丸后,头痛、头晕、胸闷、烦躁、潮热出汗、阴道不适、外阴干痛、肌肉痉挛、骨关节痛等症状明显改善;

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8、

During whole trial period, calf performance inSPC + CGM group was higher than that in milk group.

在整个试验期内, 大豆浓缩蛋白+玉米蛋白组的犊牛的生长性能优于牛奶组.

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9、

Laparoscopic colectomy for cancer is not inferior to open surgery based on 5-year data from the COST Study Group trial

腹腔镜结肠癌切除术疗效并不亚于开腹手术&基于COST的5年完整随访资料

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10、

The total effective rates for tinea pedis at week 4 were 98.36 in the trial group and 93.10 in control group; and 100 versus 98.28 at week 6, respectively.

在4周时总有效率试验组98.36%,对照组93.10%,在6周时分别为100%和98.28%。

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11、

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

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12、

The patients were divided into trial group [ PCI + normal saline ( NS ) ] and control group [ PCI + autologous bone marrow mononuclear cells ( BM-MNCs ) ] randomly.

随机分为对照组 [ PCI+生理盐水 ( NS ) ] 与试验组 [ PCI+自体骨髓单核细胞 ( BM-MNCs ) ].

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14、

When spraying the insecticide ⅲ in field, trial group tick density descended to zero and lasted for 60 days.

现场喷洒复方高效灭蜱剂Ⅲ,试验组蜱密度为0,并持效60d之久。

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16、

During whole trial period, calf performance in SPC + CGM group was higher than that in milk group.

在整个试验期内, 大豆浓缩蛋白+玉米蛋白组的犊牛的生长性能优于牛奶组.

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17、

Let's be respectful trial users, support trial access group enjoy IMBA the International Mountain Bike Association.

尽一份心力让路径对单车骑士开放,尊重路径上的其他使用者, 支持在地单车路权团体,加入[国际登山车协会](IMBA).

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18、

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.

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21、

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;

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22、

Methods: Forty-four patiens in trial group were given joint mobilization and lumbar traction on the ATA ⅱ automatic traction bed with lying on the back position;

方法:治疗组(44例)采用关节松动术,使用ATA-IID型自动牵引床,取仰卧位持续牵引治疗;

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23、

During every month, except the chest width of trial group was significantly higher than control group ( P0.05), the other body size parameters of trial group were all higher than control group but no significant differences ( P0.05).

在各月龄内,两组间除胸宽试验组显著高于对照组(P<0.05)外,其余各项体尺指标试验组均高于对照组,但没有达到显著水平(P>0.05)。

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24、

The open and single group clinical trial was composed of 2 week washout period, 8 week dosage adjustment period and 4 week dose maintenance period.

试验为单组、开放临床试验,由清洗期、剂量调整期和剂量维持期组成。

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25、

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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