Science Editor, Medical Science Monitor, International Scientific Information, Inc., Melville, NY, USA.
Med Sci Monit. 2021 Aug 30;27:e934514. doi: 10.12659/MSM.934514.
During 2020 and 2021, the COVID-19 pandemic has resulted in interruptions and cancellations of clinical trials and has delayed drug development in all areas except SARS-CoV-2 vaccine development. A further concern is the need to rapidly share anonymized datasets and improve opportunities to conduct randomized clinical trials (RCTs) in low-resource developing countries, particularly for oncology trials and for other infectious diseases. The Consolidated Standards of Reporting Trials (CONSORT) 2010 and the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) 2013 currently guide the reporting of trial protocols and completed RCTs, respectively. Extenuating circumstances or unavoidable situations may occur that are beyond the control of study sponsors and investigators. On June 21, 2021, the CONSORT and SPIRIT Extension for RCTs Revised in Extenuating Circumstance (CONSERVE) was published. The scope of CONSERVE 2021 includes modifications that have substantive implications for the feasibility, ethical conduct, scientific content, and study analysis. This Editorial aims to provide the background to CONSERVE 2021 and show how these guidelines may reduce the number of clinical trials currently being paused or discontinued due to the COVID-19 pandemic, particularly in poorly resourced and developing countries.
在 2020 年和 2021 年期间,COVID-19 大流行导致临床试验中断和取消,并推迟了除 SARS-CoV-2 疫苗开发以外的所有领域的药物开发。另一个令人担忧的问题是需要迅速共享匿名数据集,并为在资源匮乏的发展中国家开展随机临床试验(RCT)提供更多机会,特别是在肿瘤学试验和其他传染病方面。目前,《临床试验报告统一标准》(CONSORT)2010 版和《干预性临床试验标准议定书条目:建议》(SPIRIT)2013 版分别指导试验方案和已完成的 RCT 的报告。可能会出现试验发起人和研究者无法控制的极端情况或不可避免的情况。2021 年 6 月 21 日,发布了《临床试验修订版(CONSORT 和 SPIRIT 扩展版)在极端情况下的报告》(CONSERVE)。CONSERVE 2021 的范围包括对可行性、伦理行为、科学内容和研究分析具有实质性影响的修改。本社论旨在提供 CONSERVE 2021 的背景,并展示这些指南如何减少因 COVID-19 大流行而目前暂停或停止的临床试验数量,特别是在资源匮乏和发展中国家。