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2
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Editorial: Updates from the World Health Organization (WHO) on Global Treatment Recommendations for Drug-Susceptible and Multidrug-Resistant Tuberculosis.社论:世界卫生组织(WHO)关于耐多药和药物敏感结核病全球治疗建议的最新情况。
Med Sci Monit. 2021 Aug 9;27:e934292. doi: 10.12659/MSM.934292.
2
Guidelines for Reporting Trial Protocols and Completed Trials Modified Due to the COVID-19 Pandemic and Other Extenuating Circumstances: The CONSERVE 2021 Statement.因 COVID-19 大流行和其他缓解情况而修改的试验方案和已完成试验报告指南:CONSERVE 2021 声明。
JAMA. 2021 Jul 20;326(3):257-265. doi: 10.1001/jama.2021.9941.
3
Editorial: Revised World Health Organization (WHO) Terminology for Variants of Concern and Variants of Interest of SARS-CoV-2.社论:世界卫生组织(WHO)修订的关于 SARS-CoV-2 的关注变体和感兴趣变体的术语。
Med Sci Monit. 2021 Jun 21;27:e933622. doi: 10.12659/MSM.933622.
4
How COVID-19 has fundamentally changed clinical research in global health.新冠疫情如何从根本上改变了全球健康领域的临床研究。
Lancet Glob Health. 2021 May;9(5):e711-e720. doi: 10.1016/S2214-109X(20)30542-8.
5
Trends in Oncology Clinical Trials Launched Before and During the COVID-19 Pandemic.肿瘤学临床试验在 COVID-19 大流行之前和期间启动的趋势。
JAMA Netw Open. 2021 Jan 4;4(1):e2036353. doi: 10.1001/jamanetworkopen.2020.36353.
6
Effect of Dexamethasone on Days Alive and Ventilator-Free in Patients With Moderate or Severe Acute Respiratory Distress Syndrome and COVID-19: The CoDEX Randomized Clinical Trial.地塞米松对中重度 COVID-19 相关急性呼吸窘迫综合征患者存活天数和无呼吸机天数的影响:CoDEX 随机临床试验。
JAMA. 2020 Oct 6;324(13):1307-1316. doi: 10.1001/jama.2020.17021.
7
The impact of the global COVID-19 pandemic on the conduct of clinical trials: Return to normalcy by considering the practical impact of a structured ethical analysis.全球 COVID-19 大流行对临床试验开展的影响:通过考虑结构化伦理分析的实际影响,回归常态。
Br J Clin Pharmacol. 2021 Mar;87(3):837-844. doi: 10.1111/bcp.14480. Epub 2020 Jul 26.
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Implications for Design and Analyses of Oncology Clinical Trials During the COVID-19 Pandemic.2019年冠状病毒病大流行期间肿瘤学临床试验设计与分析的启示
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Ethics review of studies during public health emergencies - the experience of the WHO ethics review committee during the Ebola virus disease epidemic.突发公共卫生事件期间研究的伦理审查——世界卫生组织伦理审查委员会在埃博拉病毒病疫情期间的经验
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SPIRIT 2013 statement: defining standard protocol items for clinical trials.SPIRIT 2013 声明:定义临床试验的标准议定书项目。
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社论:报告因特殊情况(包括 COVID-19 大流行)而进行重要修改的临床试验:CONSERVE 2021。

Editorial: Reporting Clinical Trials with Important Modifications Due to Extenuating Circumstances, Including the COVID-19 Pandemic: CONSERVE 2021.

机构信息

Science Editor, Medical Science Monitor, International Scientific Information, Inc., Melville, NY, USA.

出版信息

Med Sci Monit. 2021 Aug 30;27:e934514. doi: 10.12659/MSM.934514.

DOI:10.12659/MSM.934514
PMID:34456331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8415037/
Abstract

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.

摘要

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。