Weisberg E
Clin Reprod Fertil. 1986 Apr;4(2):139-47.
Although setting up a clinical trial to test the efficacy of a method of contraception may appear to be a simple exercise, in practice, unless the aim is well delineated, the trial carefully designed, and the staff participating in the trial carefully briefed, problems will arise which prevent a successful outcome. Possible areas of bias such as selection of participants and staff prejudices must be eliminated, otherwise the value of the results may be diminished. Ethical considerations must be addressed regarding voluntary participation, information for participants, delineation of risk to participants and informed consent.
尽管开展一项临床试验来测试一种避孕方法的有效性看似是一项简单的工作,但在实际操作中,除非目标明确界定、试验精心设计且参与试验的人员得到仔细的情况介绍,否则将会出现阻碍取得成功结果的问题。必须消除可能存在的偏差领域,如参与者的选择和工作人员的偏见,否则结果的价值可能会降低。在自愿参与、向参与者提供信息、界定对参与者的风险以及知情同意等方面,必须考虑伦理因素。