Tradução de "computer-generated randomisation" em chinês
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计算机生成的随机
计算机生成的随机化
Patients without ulcers or erosive oesophagitis on endoscopy at baseline were randomly assigned by computer-generated randomisation sequence to receive famotidine 20 mg twice daily or placebo twice daily.
A computer-generated randomisation sequence, stratified by clinical centre and age group, was used to randomly assign participants to one of four treatment groups twice daily beclomethasone with beclomethasone plus albuterol as rescue (combined group); twice daily beclomethasone with placebo plus albuterol as rescue (daily beclomethasone group); twice daily placebo with beclomethasone plus albuterol as rescue (rescue beclomethasone group); and twice daily placebo with placebo plus albuterol as rescue (placebo group).
We randomly assigned patients with acute, symptomatic pulmonary embolism and a low risk of death (pulmonary embolism severity index risk classes I or II) with a computer-generated randomisation sequence (blocks of 2-4) in a 1:1 ratio to initial outpatient (ie, discharged from hospital <=24 h after randomisation) or inpatient treatment with subcutaneous enoxaparin (>=5 days) followed by oral anticoagulation (>=90 days).
Patients aged 15 years or older with confirmed second-stage T b gambiense infection were randomly assigned by computer-generated randomisation sequence to receive intravenous eflornithine for 14 days or intravenous eflornithine for 7 days with oral nifurtimox for 10 days.
Computer-generated randomisation sequence was used to allocate patients equally, via an automated telephone service, to receive 4 mg zoledronic acid as an infusion every 3-4 weeks or 1600 mg oral clodronic acid daily.
Using a computer-generated randomisation sequence, we selected 12 matched pairs of eligible hospitals.
使用计算机产生随机序列,我们选择12对匹配的医院(符合纳入标准)。
Patients were randomly allocated in a one-to-one ratio to receive erlotinib plus bevacizumab (bevacizumab group) or erlotinib plus placebo (control group) according to a computer-generated randomisation sequence by use of an interactive voice response system.
Patients were assigned (1:1:1) by computer-generated randomisation sequence to receive 24 weeks' treatment with placebo,1 μg/day paricalcitol, or 2 μg/day paricalcitol.
A computer-generated randomisation sequence was used to allocate patients randomly in a 1:1 ratio to receive amoxicillin plus clavulanic acid (3 g per day) for 8-15 days or emergency appendicectomy.
Randomisation was done centrally with a computer-generated randomisation schedule and was stratified by baseline platelet count (<= 15,000 per μL), use of treatment for immune thrombocytopenia, and splenectomy status.
In this multicentre, prospective, parallel-group, open-label trial, we used an independent, computer-generated randomisation sequence to randomly assign patients in a 1:1 ratio to procalcitonin or control groups; investigators were masked to assignment before, but not after, randomisation.
In the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study, 9795 patients aged 50-75 years with type 2 diabetes were randomly assigned by computer-generated randomisation sequence to receive fenofibrate 200 mg per day or matching placebo for 5 years' duration.
707 eligible patients were randomly assigned in a 2:1 ratio by computer-generated randomisation sequence to percutaneous closure of the LAA and subsequent discontinuation of warfarin or to warfarin treatment with a target international normalised ratio between 2.0 and 3.0.
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