Suppr超能文献

早期青光眼临床试验中的安慰剂效应。

The placebo effect in early-phase glaucoma clinical trials.

作者信息

Sharpe R Allan, Nelson Lindsay A, Stewart Jeanette A, Stewart William C

机构信息

Department of Ophthalmology, Medical University of South Carolina , Charleston, SC , USA and.

出版信息

Curr Eye Res. 2015 May;40(6):653-6. doi: 10.3109/02713683.2014.946519. Epub 2014 Aug 12.

Abstract

PURPOSE

To analyze the extent and prevalence of the placebo effect in prior early-phase glaucoma clinical studies.

METHODS

Articles were evaluated on phase I and II trials of glaucoma medicines that became commercially available after 1977 with a placebo arm that involved glaucoma patients.

RESULTS

We included 23 studies with 23 treatment arms with a total of 1703 patients in articles evaluating 10 different glaucoma medications. This study showed that at 8 AM (n = 18), the average decrease in placebo from untreated baseline was 2.3 ± 1.6 mm Hg (9%), while for the diurnal curve (n = 17), the mean decrease was 1.4 ± 1.1 mm Hg (6%). At 8 AM, 8/18 treatment arms had greater than 2 mm Hg intraocular pressure (IOP) decrease, and all had at least some reduction in IOP. For the diurnal curve, 4 of 17 studies had reduced IOP greater than 2 mm Hg. One treatment arm had no placebo effect.

CONCLUSIONS

This study suggests that a placebo effect is common in glaucoma clinical trials and potentially could limit the ability to evaluate the efficacy of a new medicine.

摘要

目的

分析既往早期青光眼临床研究中安慰剂效应的程度和普遍性。

方法

对1977年后上市的青光眼药物的I期和II期试验文章进行评估,这些试验设有涉及青光眼患者的安慰剂组。

结果

我们纳入了23项研究,共23个治疗组,总计1703例患者,这些研究评估了10种不同的青光眼药物。该研究表明,上午8点时(n = 18),安慰剂组相较于未治疗基线的平均眼压降低为2.3±1.6 mmHg(9%),而对于昼夜眼压曲线(n = 17),平均降低为1.4±1.1 mmHg(6%)。上午8点时,18个治疗组中有8个组眼压降低超过2 mmHg,且所有组眼压均至少有一定程度降低。对于昼夜眼压曲线,17项研究中有4项研究眼压降低超过2 mmHg。有一个治疗组无安慰剂效应。

结论

本研究提示,安慰剂效应在青光眼临床试验中很常见,可能会限制评估新药疗效的能力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验