Janssen Pharmaceutical Research & Development, LLC, Titusville, NJ 08560, USA.
J Pain. 2013 Apr;14(4):405-11. doi: 10.1016/j.jpain.2012.12.011. Epub 2013 Feb 28.
ClinicalTrials.gov is a registry and results database of federally and privately supported clinical trials conducted worldwide. We sought to answer: what are the characteristics of pain trials; how frequently are these trials stopped and why; what is the magnitude of attrition due to lack of efficacy or adverse events; and whether the withdrawal rates depend on pain syndrome. To facilitate this and subsequent studies, we have developed a system called Sherlock that automatically downloads data from ClinicalTrials.gov into a relational database. We included pain interventional trials. To evaluate attrition, we restricted consideration to prospective randomized, parallel, double-blind, placebo-controlled trials. Of the 82,867 trials, 6% reported results and 5.6% terminated before the planned number of subjects was accrued. Of these early terminations, 38% were due to enrollment difficulties. In the placebo arms, 3.8% of participants withdrew due to lack of efficacy and 4.9% due to adverse events, with proportions differing among pain conditions. Compared with migraine trials, in fibromyalgia trials 5.1% more participants withdrew due to lack of efficacy (95% confidence interval [CI], 2.5-7.8%), and 6.4% more withdrew due to adverse events (95% CI, 4.3-8.6%). Nonsteroidal anti-inflammatory drugs were the treatment class with the lowest adverse events withdrawals. Recruitment challenges account for the largest proportion of noncompleted trials. Attrition rates differ across pain conditions. Migraine studies had the lowest withdrawal rate. Tools like Sherlock facilitate conducting research in the ClinicalTrials.gov registry.
ClinicalTrials.gov registry enables researchers to get a snapshot of a specific field and observe changes over time in trial design, including numbers of subjects accrued, and it can inform clinical trial design. We learned that recruitment challenges account for the largest proportion of noncompleted trials, attrition rates differed across pain conditions, and migraine studies had the lowest withdrawal rate.
ClinicalTrials.gov 是一个注册和结果数据库,收录了全球范围内由联邦政府和私人机构支持的临床试验。我们试图回答以下问题:疼痛试验有哪些特点;这些试验有多少被停止,原因是什么;因缺乏疗效或不良反应而导致的脱落率是多少;撤回率是否取决于疼痛综合征。为了便于回答这些问题和开展后续研究,我们开发了一个名为 Sherlock 的系统,该系统可以自动从 ClinicalTrials.gov 下载数据到关系数据库中。我们纳入了疼痛干预试验。为了评估脱落率,我们只考虑前瞻性随机、平行、双盲、安慰剂对照试验。在 82867 项试验中,有 6%报告了结果,5.6%在计划入组人数完成之前终止。在这些早期终止的试验中,38%是由于入组困难。在安慰剂组中,3.8%的参与者因缺乏疗效而退出,4.9%因不良反应而退出,不同疼痛状况的比例不同。与偏头痛试验相比,纤维肌痛试验中因缺乏疗效而退出的参与者比例增加了 5.1%(95%置信区间[CI],2.5%-7.8%),因不良反应而退出的参与者比例增加了 6.4%(95% CI,4.3%-8.6%)。非甾体抗炎药是不良反应退出率最低的治疗类别。招募挑战占未完成试验的最大比例。脱落率因疼痛状况而异。偏头痛研究的退出率最低。像 Sherlock 这样的工具可以方便地在 ClinicalTrials.gov 注册中心进行研究。
ClinicalTrials.gov 注册中心使研究人员能够了解特定领域的概况,并观察试验设计随时间的变化,包括入组人数的变化,还可以为临床试验设计提供信息。我们了解到,招募挑战占未完成试验的最大比例,脱落率因疼痛状况而异,偏头痛研究的退出率最低。