METHODS: We conducted a multicenter, randomized, double - blind, parallel - treatment, placebo - controlled study in Japan.
方法：在日本进行一项多中心随机双盲对比治疗的安慰剂对照研究。
Efficacy and Safety of Prophylactic Large Dose of Tranexamic Acid in Spine Surgery: a Prospective, Randomized, Double-Blind, Placebo-Controlled Study.
预防性大剂量氨甲环酸在脊柱外科中的疗效和安全性：一个前瞻性，随机，双盲，安慰剂对照的研究。
Methods A randomized double-blind parallel controlled clinical trial was conducted.
方法本研究采用随机、双盲、平行对照的临床研究方法。
Methods a multicenter, double-blind, randomized controlled trial was conducted.
方法用多中心随机双盲对照试验。
DESIGN: a completely randomized, double blind controlled trial was conducted.
设计：完全随机双盲实验对照研究。
Methods:this was a randomized, double blind controlled trial.
方法：采用随机双盲对照研究。
Methods: a randomized double-blind controlled clinical trial (RCT) was conducted.
方法：随机双肓对照临床试验(rct)。
Methods: A randomized and double-blind controlled clinical trial was conducted for smoking cessation.
方法：采用随机、双盲、安慰剂平行对照研究。
METHODS: We conducted a multicenter, randomized, double-blind, parallel-treatment, placebo-controlled study in Japan.
方法：在日本进行一项多中心随机双盲对比治疗的安慰剂对照研究。
Methods It is a randomized double-blind parallel controlled multiple-centered clinical study design. The inpatients 161 cases who accorded program and needed parental nutrition enter this study.
方法本研究为随机双盲、平行对照、多中心实验设计，符合研究方案、需要肠外营养的住院病人161例进入本研究。
Methods: a multicenter, randomized, double blind, and placebo controlled clinical study was performed.
方法本次为一中心，随机，双盲，安慰剂对照临床观察。
Leflunomide was evaluated in a randomized, double-blind, placebo-controlled study in active ankylosing spondylitis but was not found to be effective.
来氟米特通过随机双盲安慰剂对照试验研究表明，对强直性脊柱炎急性期没有效果。
These patients had acne vulgaris ranging from mild to severe and were a subgroup of patients from phase 3, randomized, double-blind, vehicle-controlled, multicenter clinical trials.
这些患者有轻到重度痤疮，是基质对照随机双盲多中心3期临床试验的一个亚组。
METHODS: It was a randomized, double blind, double model, parallel controlled clinical trial.
方法：采用随机、双盲双模拟、平行对照方法。
METHODS: A prospective multi-center, randomized , double blind, controlled clinical trial of serrapeptase enteric-coated tablets was conducted.
方法：用前瞻性随机双盲双模拟对照多中心试验设计，以进口舍雷肽酶肠溶片为阳性对照药。
A 24 week multicentre, double-blind, randomized, placebo-controlled trial.
24周的多中心，随机，双盲，安慰剂对照试验。
You can test an intervention, such as an experimental drug or an educational program, in the purest way (a double-blind randomized controlled trial).
你可以测试一个干预，比如实验药物或一个教育计划，以最纯粹的方式(双盲随机对照试验)。
The data are from an extension study of a randomized, double-blind, placebo-controlled trial.
这些数据来自一个随机、双盲、安慰剂对照试验、根据研究。
Randomized, there are placebo-controlled, double-blind, multi-center clinical trials to prove efficacy is a reliable method.
随机分组、有安慰剂对照、双盲、多中心的临床试验，才是证明疗效的可靠方法。
New hope for hundreds of thousands of people suffering from chronic sciatica was revealed this week in a Phase II randomized, double-blind, placebo-controlled trial.
本周在一项II期随机、双盲、安慰剂对照试验中揭晓了几十万慢性坐骨神经痛患者的治疗新希望。
MATERIALS and METHODS: This was a randomized, double-blind, placebo controlled, parallel group, multicenter study.
材料和方法：这是一项随机、对照、双盲、平行分组、多中心的研究。
A double-blind, randomized, placebo-controlled trial.
双盲，随机，安慰剂对照试验。
Methods This is a randomized, double blind, double-dummy, multi-center, parallel positive controlled clinical study.
方法用随机化、双盲、双模拟、多中心、阳性药平行对照研究方法。
Patients with haematological malignancies receiving intensive chemotherapy and requiring hospitalization were randomized in a double-blind, placebo-controlled single-centre trial.
入院接受密集化疗的血液学恶性肿瘤的病人被随机分为两组，在单中心实验中用双盲法处理安慰剂组和控制组。
All the sub-studies were randomized, placebo-controlled, double-blind and had a parallel-group design.
所有研究均为随机、空白- 对照、双盲的平行设计试验。
METHODS: a randomized, double-blind, controlled and dosage-adjusted clinical trial was conducted.
方法：采用随机、双盲、对照、剂量可调整性研究。
In this randomized, double-blind, placebo-controlled study, we examined 20 healthy volunteers who ingested 12 mg AXT or placebo capsules over a 4-week period.
在这项随机，双盲，安慰剂对照研究中，我们研究了20名健康志愿者超过4周期间摄入12毫克的或安慰剂胶囊。
In this randomized, double-blind, placebo-controlled study, we examined 20 healthy volunteers who ingested 12 mg AXT or placebo capsules over a 4-week period.
在这项随机，双盲，安慰剂对照研究中，我们研究了20名健康志愿者超过4周期间摄入12毫克的或安慰剂胶囊。
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