Epidemiology Unit, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid, Avda Reyes Católicos 2, E-28040, Madrid, Spain.
Eur J Clin Pharmacol. 2021 Apr;77(4):539-546. doi: 10.1007/s00228-020-03030-8. Epub 2020 Oct 26.
To assess, with all available trial information, whether the assessment of the PRECIS-2 nine domains could provide a clear distinction between medicine masked pragmatic randomized controlled trials (pRCTs) and open-label pRCTs.
A search was conducted of participant-level pRCTs on medicines published on 25 influential medical journals in July 2018-December 2019. All pre-licensing (phases 1-3) and cluster pRCTs were excluded. All trials' available reports were searched through the published article information, Google Scholar, and trial websites. Instead of providing a score to each PRECIS-2 domain, these were classified as E (explanatory), N (neutral), or P (pragmatic).
Of 128 pRCTs, 18 (14%) were participant-level pRCTs on medicines. The full trial protocol was available for 14 trials; 12 had published the protocol and nine had additional reports published. All trials were prospectively registered, and none was funded by industry. Ten and eight were masked and open-label trials, respectively. Masked pRCTS had 34% of pragmatic and 60% of explanatory domains; open-label pRCTS had 45% pragmatic and 45% explanatory domains. Among the 10 masked trials, only one had a majority of five pragmatic domains; among the eight open-label trials, four had a majority of six or five pragmatic domains. "Follow-up" was considered explanatory in the 18 pRCTs; "primary analysis" was pragmatic in 17 pRCTs.
The PRECIS-2 tool seems not to be sensitive enough to clearly discriminate between medicine masked pRCTs and open-label pRCTs. When conducting systematic reviews, it is suggested that the PRECIS-2 tool should not be used to support placing masked trials in the pragmatic side of the explanatory/pragmatic continuum.
利用所有可用的试验信息,评估 PRECIS-2 九个领域的评估是否能够清晰地区分医学掩盖的实用随机对照试验(pRCT)和开放标签 pRCT。
对 2018 年 7 月至 2019 年 12 月发表在 25 种有影响力的医学期刊上的药物参与者水平 pRCT 进行了检索。排除所有预先许可(第 1-3 阶段)和簇 RCT。通过发表文章信息、Google Scholar 和试验网站搜索所有试验的可用报告。这些试验不是对每个 PRECIS-2 领域进行评分,而是将其分为 E(解释性)、N(中立)或 P(实用性)。
在 128 项 pRCT 中,有 18 项(14%)是关于药物的参与者水平 pRCT。14 项试验提供了完整的试验方案;12 项试验已公布方案,9 项试验有额外报告公布。所有试验均为前瞻性注册,且均无行业资助。10 项为掩蔽试验,8 项为开放标签试验。掩蔽 pRCT 有 34%的实用性和 60%的解释性领域;开放标签 pRCT 有 45%的实用性和 45%的解释性领域。在 10 项掩蔽试验中,只有一项有 5 个实用性领域的多数;在 8 项开放标签试验中,有 4 项有 6 个或 5 个实用性领域的多数。在 18 项 pRCT 中,“随访”被认为是解释性的;在 17 项 pRCT 中,“主要分析”是实用性的。
PRECIS-2 工具似乎不够敏感,无法清晰地区分医学掩盖的 pRCT 和开放标签 pRCT。在进行系统评价时,建议不要使用 PRECIS-2 工具将掩蔽试验置于解释性/实用性连续体的实用性一侧。