Titlebook: Randomised Controlled Clinical Trials; Christopher J. Bulpitt Book 1996Latest edition Springer Science+Business Media New York 1996 drugs.

游牧

书目名称Randomised Controlled Clinical Trials影响因子(影响力)




书目名称Randomised Controlled Clinical Trials影响因子(影响力)学科排名




书目名称Randomised Controlled Clinical Trials网络公开度




书目名称Randomised Controlled Clinical Trials网络公开度学科排名




书目名称Randomised Controlled Clinical Trials被引频次




书目名称Randomised Controlled Clinical Trials被引频次学科排名




书目名称Randomised Controlled Clinical Trials年度引用




书目名称Randomised Controlled Clinical Trials年度引用学科排名




书目名称Randomised Controlled Clinical Trials读者反馈




书目名称Randomised Controlled Clinical Trials读者反馈学科排名

准则

LAPSE

Recruitment of Subjects,The recruitment of subjects must be considered very carefully to ensure that sufficient persons with the characteristics required by the investigators are enrolled within an appropriate period of time. The number of subjects is of great importance and was discussed in chapter 6.

Reservation

愚笨

obnoxious

,The Conduct of the Trial — Good Clinical Practice,are foreseen and taken into account of prior to the start of the trial and those that are unexpected. Murphy’s law states, “..” This law has been attributed to captain E Murphy, a development engineer, who applied it first to an individual technician saying, “.” [215].

某人

BAIL

Early Trials on New Drugs, three phases of early trials: trials to determine safety and early clinical pharmacology (phase I); trials to determine clinical efficacy and further clinical pharmacology (phase II); and trials for the early clinical development of the drug (phase III). A drug regulatory authority may be involved in these early trials.

Brittle

不能和解

asurement of the benefit:risk comparison; determination ofcost- effectiveness and cost utility; stopping rules for trials;meta-analysis and subgroup analysis are all new sections. Thereferences are expanded from 305 to 512 and include the recentadvances in trial design, such as the .n.-of-1 trials a