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after randomization
Vertaling van "after randomization" in Chinees
随机分组后
随机化后
Treatment was started after randomization and ended 30 days later.
随机分组后开始治疗，并在30天后结束。
Four years after randomization, overall survival was similar in the two study groups.
在随机分组后4年，两个研究组的总生存率相似。
The rates of adverse events and death after randomization did not differ significantly among the groups, although comparisons were based on small numbers of patients, especially during the final 16 weeks.
随机化后，各组间的不良事件发生率和死亡率无显著差异，尽管这些比较是基于少数患者，尤其是最后16周内。
There were no significant differences in the inci- dence of any event after randomization, except for a higher rate of bacteremia in the hypothermia group than in the normothermia group.
在发病的任何事件随机化后没有显着差异，除了在低温组比常温组一个较高菌血症的增长率。
The primary end point was a composite of in-hospital death and embolic events that occurred within 6 weeks after randomization.
主要终点是发生在随机分组后6周内的院内死亡以及栓塞事件的复合终点。
Six years after randomization, endovascular and open repair of abdominal aortic aneurysm resulted in similar rates of survival.
随机分组后6年，腹主动脉瘤的腔内修复术和开腹修复术取得了相似的（患者）生存率。
The primary outcome was death from any cause 28 days after randomization.
主要转归为随机分组后28天任何原因所致死亡。
The primary outcome for this guideline was total mortality up to 120 days after randomization.
主要为这一指南是随机分组后的总死亡率高达120天。
The primary outcome measure was either death or end-stage kidney failure (dependence on dialysis) at 90 days after randomization.
主要转归评定为随机分组后90天时的死亡或终末期肾衰竭（依赖透析）情况。
The primary outcome was the rate of death at 28 days after randomization; secondary end points included the number of days without need for organ support and the occurrence of adverse events.
主要转归是随机分组后28天的死亡率，次要终点包括不需要器官支持的天数和不良事件的发生率。
There were no significant differences in the incidence of any event after randomization, except for a higher rate of bacteremia in the hypothermia group than in the normothermia group.
除低温组菌血症的发生率较高外，随机分组后其它情况差异无显著性。
The median dose of amiodarone and placebo was 300 mg per day three months after randomization and remained so throughout the study.
在随机分组后3月直至研究结束氨碘酮组和安慰剂组的中位数剂量为300毫克。
The primary composite end point was stroke, myocardial infarction, or death from any cause during the periprocedural period or any ipsilateral stroke within 4 years after randomization.
主要复合终点是围操作期发生的卒中、心肌梗死，或任何原因导致的死亡，或随机分组后4年内的任何同侧卒中。
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Synoniemen voor after randomization in het Engels
Woord & uitdrukking van de dag
Afbeelding van de dag
Resultaten: 30. Exact: 30. Verstreken tijd: 17 ms.
