首页> 外文期刊>The journal of pain: official journal of the American Pain Society >Research Design Characteristics of Published Pharmacologic Randomized Clinical Trials for Irritable Bowel Syndrome and Chronic Pelvic Pain Conditions: An ACTTION Systematic Review
【24h】

Research Design Characteristics of Published Pharmacologic Randomized Clinical Trials for Irritable Bowel Syndrome and Chronic Pelvic Pain Conditions: An ACTTION Systematic Review

机译:发表药物随机临床试验的研究设计特征肠辨别综合征和慢性盆腔疼痛条件:震动系统综述

获取原文
获取原文并翻译 | 示例
           

摘要

Chronic pain conditions occurring in the lower abdomen and pelvis are common, often challenging to manage, and can negatively affect health-related quality of life. Methodological challenges in designing randomized clinical trials (RCTs) for these conditions likely contributes to the limited number of available treatments. The goal of this systematic review of RCTs of pharmacologic treatments for irritable bowel syndrome and 3 common chronic pelvic pain conditions are to: 1) summarize the primary end points and entry criteria, and 2) evaluate the clarity of reporting of important methodological details. In total, 127 RCTs were included in the analysis. The most common inclusion criteria were a minimum pain duration (81%), fulfilling an established diagnostic criteria (61%), and reporting a minimum pain intensity (42%). Primary end points were identified for only 57% of trials. These end points, summarized in this article, were highly variable. The results of this systematic review can be used to inform future research to optimize the entry criteria and outcome measures for pain conditions occurring in the lower abdomen and pelvis, to increase transparency in reporting to allow for proper interpretation of RCT results for clinical and policy applications, and to facilitate the aggregation of data in meta-analyses.
机译:在下腹部和骨盆中发生的慢性疼痛条件是常见的,往往是挑战的管理,并且可能对健康有关的生活质量产生负面影响。为这些条件设计随机临床试验(RCT)的方法论挑战可能有助于有限数量的可用治疗方法。这种系统评价对肠易激综合征和3种常见的慢性骨盆疼痛条件的调药治疗的RCT的目标是:1)总结主要终点和入门标准,2)评估报告重要方法细节的清晰度。总共包括127个RCT分析。最常见的包含标准是最小疼痛持续时间(81%),满足既定的诊断标准(61%),报告最小疼痛强度(42%)。仅确定了初级终点仅为57%的试验。本文总结的这些终点是高度变化的。该系统审查的结果可用于通知未来的研究,以优化下腹部和骨盆中发生的疼痛病症的进入标准和结果测量,以提高报告的透明度,以便正确地解释临床和政策应用的RCT结果,并促进Meta分析中数据的聚合。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号