Carpenter William T, Appelbaum Paul S, Levine Robert J
Maryland Psychiatric Research Center, Univeristy of Maryland School of Medicine, USA.
Am J Psychiatry. 2003 Feb;160(2):356-62. doi: 10.1176/appi.ajp.160.2.356.
The authors' goal was to consider ethical approaches to placebo-controlled clinical trials in the light of the evolving Declaration of Helsinki, with special attention to applications to research on schizophrenia.
They review the Helsinki position on placebos, including the 2002 Clarification, exploring the potential negative effects of banning placebos in studies involving conditions for which at least partially effective treatments exist. The Clarification is examined as an approach to this issue that, in contrast to earlier formulations, better acknowledges the complexity of clinical research and the need for protocol-specific determinations. Placebo controls in schizophrenia studies are used to illustrate issues relevant to all clinical research on therapeutic interventions.
The Helsinki Clarification provides a basis for operationalizing criteria for review of placebo use in clinical trials. Six criteria are proposed for judging the ethical acceptability of placebo controls, including the likelihood that the intervention being tested will have clinically significant advantages over existing treatments, the presence of compelling reasons for placebo use, subject selection that minimizes the possibility of serious adverse consequences, and a risk-versus-benefit analysis that favors the advantages from placebo use over the risks to subjects.
The Helsinki Clarification constitutes an important advance in international approaches to placebo use, requiring protocol-by-protocol judgments on complex issues of clinical research ethics. When operationalized, it provides review boards with a useful methodology for reaching determinations on the appropriateness of placebo controls in particular studies.
作者的目标是根据不断演变的《赫尔辛基宣言》来思考安慰剂对照临床试验的伦理方法,特别关注其在精神分裂症研究中的应用。
他们回顾了《赫尔辛基宣言》关于安慰剂的立场,包括2002年的《澄清声明》,探讨了在涉及至少有部分有效治疗方法的疾病研究中禁止使用安慰剂可能产生的负面影响。对《澄清声明》进行了审视,认为它是解决这一问题的一种方法,与早期的表述相比,它更好地认识到了临床研究的复杂性以及针对特定方案进行判定的必要性。以精神分裂症研究中的安慰剂对照为例,来说明与所有治疗性干预措施的临床研究相关的问题。
《赫尔辛基宣言澄清声明》为实施临床试验中安慰剂使用的审查标准提供了依据。提出了六项判断安慰剂对照伦理可接受性的标准,包括所测试的干预措施比现有治疗方法具有临床显著优势的可能性、使用安慰剂的令人信服的理由、选择受试者时尽量减少严重不良后果的可能性,以及一项风险与效益分析,该分析表明使用安慰剂的优势大于对受试者的风险。
《赫尔辛基宣言澄清声明》是国际上在安慰剂使用方法上的一项重要进展,要求针对临床研究伦理的复杂问题逐案进行判断。在实际操作时,它为审查委员会提供了一种有用的方法,以便就特定研究中安慰剂对照的适用性做出判定。