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Randomized double-blind placebo-controlled trial of homoeopathic 'proving' for Belladonna C30.顺势疗法“验证”颠茄C30的随机双盲安慰剂对照试验。
J R Soc Med. 1998 Nov;91(11):579-82. doi: 10.1177/014107689809101108.
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J Psychosom Res. 1993 Dec;37(8):851-60. doi: 10.1016/0022-3999(93)90174-e.
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引用本文的文献

1
The conclusion that 'ultramolecular homeopathy has no observable clinical effects' is not supported by the data.“超分子顺势疗法没有可观察到的临床效果”这一结论没有得到数据支持。
Br J Clin Pharmacol. 2004 Sep;58(3):340-1. doi: 10.1111/j.1365-2125.2004.02127.x.
2
Ultramolecular homeopathy has no observable clinical effects. A randomized, double-blind, placebo-controlled proving trial of Belladonna 30C.超分子顺势疗法没有可观察到的临床效果。一项关于颠茄30C的随机、双盲、安慰剂对照验证试验。
Br J Clin Pharmacol. 2003 Nov;56(5):562-8. doi: 10.1046/j.1365-2125.2003.01900.x.

本文引用的文献

1
Does a highly diluted homoeopathic drug act as a placebo in healthy volunteers? Experimental study of Belladonna 30C in double-blind crossover design--a pilot study.高度稀释的顺势疗法药物在健康志愿者中是否起安慰剂作用?颠茄30C双盲交叉设计的实验研究——一项初步研究。
J Psychosom Res. 1993 Dec;37(8):851-60. doi: 10.1016/0022-3999(93)90174-e.

顺势疗法“验证”颠茄C30的随机双盲安慰剂对照试验。

Randomized double-blind placebo-controlled trial of homoeopathic 'proving' for Belladonna C30.

作者信息

Goodyear K, Lewith G, Low J L

机构信息

School of Medicine, University Medicine, University of Southampton, UK.

出版信息

J R Soc Med. 1998 Nov;91(11):579-82. doi: 10.1177/014107689809101108.

DOI:10.1177/014107689809101108
PMID:10325874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1296951/
Abstract

Homoeopathic drug pictures are developed by recording the symptomatic effects of homoeopathic remedies given to healthy volunteers (a 'proving'). In a double-blind randomized controlled trial we tested the hypothesis that individuals using an infinitesimal dilution of Belladonna (thirtieth potency, C30) would record more true symptoms, on a questionnaire that contained both true and false Belladonna proving symptoms, than those receiving placebo. 60 volunteers entered the study and 47 completed data collection. We were unable to distinguish between Belladonna C30 and placebo using our primary outcome measure. For the secondary outcome measure we analysed the number of individuals who proved to the remedy according to our predefined criteria: 4 out of 19 proved in the Belladonna C30 group and 1 out of 27 in the placebo group (difference not statistically significant). This pilot study does not demonstrate a clear proving reaction for Belladonna C30 versus placebo, but indicates how the question might be further investigated.

摘要

顺势疗法药物图像是通过记录给予健康志愿者的顺势疗法药物的症状效应(“验证”)而形成的。在一项双盲随机对照试验中,我们检验了这样一个假设:在一份包含真、假颠茄验证症状的问卷上,使用颠茄极微稀释液(三十次方药力,C30)的个体记录的真实症状会比接受安慰剂的个体更多。60名志愿者参与了该研究,47名完成了数据收集。使用我们的主要结局指标,我们无法区分颠茄C30和安慰剂。对于次要结局指标,我们分析了根据我们预先定义的标准对该药物产生验证反应的个体数量:颠茄C30组19人中有4人产生验证反应,安慰剂组27人中有1人产生验证反应(差异无统计学意义)。这项初步研究并未表明颠茄C30与安慰剂相比有明显的验证反应,但指出了该问题可如何进一步研究。