临床试验中盲性的评估

Heejung Bang , Liyun Ni , Clarence E Davis
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引用次数: 385

摘要

在许多临床试验中,盲法的成功是一个基本问题。如果违反了这一重要假设,审判的有效性就可能受到质疑。尽管每年有数以万计的表面上的双盲试验被进行,研究者也承认盲法的重要性,但很少有人讨论如何衡量盲法的有效性。一些已发表的论文提出了评估盲法成功与否的方法,但没有一种方法是常用的或被视为标准的。本文探讨了一种评估临床试验中盲法成功与否的新方法。将提出的盲指标按- 1到1的区间缩放,1表示完全不盲,0表示与完全盲一致,- 1表示猜测相反,可能与解盲有关。它有能力检测相对较低程度的致盲、反应偏差和两只手臂的不同行为。该方法已应用于一组老年人降胆固醇药物的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of blinding in clinical trials

Success of blinding is a fundamental issue in many clinical trials. The validity of a trial may be questioned if this important assumption is violated. Although thousands of ostensibly double-blind trials are conducted annually and investigators acknowledge the importance of blinding, attempts to measure the effectiveness of blinding are rarely discussed. Several published papers proposed ways to evaluate the success of blinding, but none of the methods are commonly used or regarded as standard. This paper investigates a new approach to assess the success of blinding in clinical trials. The blinding index proposed is scaled to an interval of −1 to 1, 1 being complete lack of blinding, 0 being consistent with perfect blinding and −1 indicating opposite guessing which may be related to unblinding. It has the ability to detect a relatively low degree of blinding, response bias and different behaviors in two arms. The proposed method is applied to a clinical trial of cholesterol-lowering medication in a group of elderly people.

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