Clinical trials are sets of tests performed for medical research and drug development which is used to extract safety and efficacy data.
行业： 医疗设备; 制药
临床试验设计既不参与个人也研究人员不知道哪些参与者正在接受实验药物和其中正在接受安慰剂 (或另一种疗法)。双盲试验被认为是产生客观的结果，因为医生和有关的实验性药物参与者的期望不会影响结果 ；也称为双蒙面的研究。看到盲法的研究、 单盲的研究和安慰剂。 ...
改性的一种药物时以另一种药物的方式管理的影响。效果可能会增加或减少的行动的两种物质，或它可能不是通常与两种药物相关的不良影响。
摘要的参与者甄选标准 ；包括纳入和排除标准。
签约入研究参与者的行为。一般这一过程涉及评价研究的资格标准的参与者和经历知情同意过程。
A control is the nature of the intervention control.
Overall outcome that the protocol is designed to evaluate. Common endpoints are severe toxicity, disease progression, or death.
1. Information gathered at the beginning of a study from which variations found in the study are measured. 2. A known value or quantity with which an unknown is compared when measured or assessed. 3. ...
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