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一项多中心、随机、双盲、对照剂量探索研究,评估 NGX-4010(一种高浓度辣椒素贴片)治疗带状疱疹后神经痛的疗效。

A multicenter, randomized, double-blind, controlled dose finding study of NGX-4010, a high-concentration capsaicin patch, for the treatment of postherpetic neuralgia.

机构信息

Lifetree Clinical Research and Pain Clinic, Salt Lake City, Utah 84106, USA.

出版信息

J Pain. 2010 Oct;11(10):972-82. doi: 10.1016/j.jpain.2010.01.270. Epub 2010 Jul 24.

Abstract

UNLABELLED

Postherpetic neuralgia (PHN) is a painful complication of acute herpes zoster. This multicenter, double-blind, controlled study randomized 299 PHN patients to receive either NGX-4010, a high-concentration capsaicin (8%) patch, or a low-concentration capsaicin (0.04%) control patch for 30, 60, or 90 minutes. The mean percent reductions in NPRS score from baseline to weeks 2 through 8 were significantly greater in the total NGX-4010 group (26.5%, P = .0286) and the 90-minute NGX-4010 group (27.8%, P = .0438) compared to the pooled control group (17.3%). After review of the data suggested a difference between genders in reporting of pain scores and a higher proportion of males (61%) in the 60-minute NGX-4010 group, post hoc gender-stratified analyses were performed and showed that the 60-minute NGX-4010 group also had a significantly larger mean percent reduction in average pain scores (28.0%, P = .0331). Pain reduction in the 30-minute NGX-4010 group, although similar in magnitude to the other doses, was not significantly different from control in either of these analyses. Similar results were observed during weeks 2 through 12. Most treatment-emergent adverse events were application-site specific, transient and mostly mild to moderate in severity.

PERSPECTIVE

This article reports the safety and efficacy of NGX-4010 applied for 3 different durations (30, 60, or 90 minutes) in patients with PHN. The results identified the 60-minute duration as the dose to be evaluated in subsequent studies and identified a gender effect on reported changes in pain.

摘要

背景

带状疱疹后神经痛(PHN)是急性带状疱疹的一种疼痛并发症。这项多中心、双盲、对照研究将 299 名 PHN 患者随机分为 NGX-4010 组(高浓度辣椒素[8%]贴剂)或对照低浓度辣椒素(0.04%)贴剂组,分别贴用 30、60 或 90 分钟。从基线到第 2 周到第 8 周,NPRS 评分的平均百分比下降在总 NGX-4010 组(26.5%,P =.0286)和 90 分钟 NGX-4010 组(27.8%,P =.0438)显著大于汇总对照。在数据审查表明报告疼痛评分的性别差异和 60 分钟 NGX-4010 组中男性比例较高(61%)后,进行了事后性别分层分析,结果表明 60 分钟 NGX-4010 组平均疼痛评分的平均百分比也有显著更大的下降(28.0%,P =.0331)。尽管 30 分钟 NGX-4010 组的疼痛缓解程度相似,但在这些分析中与对照相比均无显著差异。在第 2 周到第 12 周期间观察到类似的结果。大多数治疗突发不良事件是应用部位特异性的、短暂的,并且大多数为轻度至中度。

观点

本文报告了 NGX-4010 在 PHN 患者中应用 3 种不同时间(30、60 或 90 分钟)的安全性和有效性。结果确定了 60 分钟的时间作为后续研究中要评估的剂量,并确定了报告的疼痛变化的性别效应。

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