COVID-19对耳鼻喉科研究的影响:对已停止试验的横断面分析

Brayden Rucker, Nicholas B. Sajjadi, L. Brame, M. Vassar, M. Hartwell
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Investigators performed screening and data extraction in a duplicate, masked fashion. Trials resulting from the search were extracted for trial status, condition treated, enrollment number, funding, study type, study design, last update posted date, and trial location. Trials that explicitly mentioned COVID-19 as a reason for discontinuation or suspension were coded as such. For trials that did not explicitly mention COVID-19, we coded the reason provided from ClinicalTrials.gov. The Oklahoma State University Center for Health Science Institutional Review Board determined that this project did not qualify as human subject research. Results A total of 1,777 CTs met the inclusion criteria, and 223 CTs were discontinued between January 1, 2020 and August 1, 2021. Thirty-three (14.8%) of the 223 CTs reported discontinuation explicitly due to the COVID-19 pandemic. The 33 studies had 1,715 participants enrolled in total. Among the primary interventions, 11 (33.3%) were devices, 10 (30.3%) were drugs, 5 (15.2%) were behavioral, 4 (12.1%) were diagnostic tests, 1 (3.0%) was dietary, and 2 (6.1%) were labeled as “other.” Regarding the CT location, 20 (60.6%) were conducted in the United States, and 13 (39.4%) were conducted internationally. Of the 33 CTs, 19 (57.6%) were suspended, 9 (27.3%) were terminated, and 5 (15.2%) were withdrawn. The overall most common reason for trial disruption was recruitment difficulties (24.2%). Median enrollment for discontinued trials due to COVID-19 was 37 (interquartile range [IQR], 19–71) and for other reasons was 6 (IQR, 0–27), for which the Mann–Whitney test showed a statistically significant difference between the two (z=−3.913, p<0.001). There were no significant associations between trial location, funding source, randomization, or whether a study involved masked vs unmasked participants. 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引用次数: 2

摘要

新冠肺炎疫情导致科研人员招聘困难、供应链短缺、经费短缺等,降低了医学研究能力。耳鼻喉科的临床实践尤其受到影响,因为选择性手术的减少,如面部整形手术和声带注射。本研究的主要目的是研究2019冠状病毒病(COVID-19)大流行对耳鼻喉科临床试验(ct)中断的程度。方法于2021年8月1日,我们在ClinicalTrials.gov网站上对常见耳鼻喉科疾病相关的ct进行了系统检索。我们利用2020年1月1日至2021年8月1日的日期范围来确定所有可能受COVID-19大流行影响的试验。调查人员以重复的蒙面方式进行筛选和数据提取。从检索中提取试验状态、治疗条件、入组编号、资助、研究类型、研究设计、最后更新发布日期和试验地点。明确将COVID-19作为终止或暂停原因的试验被编码为此类试验。对于没有明确提到COVID-19的试验,我们编码了ClinicalTrials.gov提供的原因。俄克拉荷马州立大学健康科学中心机构审查委员会决定,该项目不符合人体实验研究的资格。结果共有1777例ct符合纳入标准,其中223例在2020年1月1日至2021年8月1日期间停用。223个ct中有33个(14.8%)报告明确因COVID-19大流行而中断。这33项研究共纳入了1715名参与者。在主要干预措施中,11项(33.3%)为设备,10项(30.3%)为药物,5项(15.2%)为行为,4项(12.1%)为诊断测试,1项(3.0%)为饮食,2项(6.1%)为“其他”。CT定位方面,20例(60.6%)在美国进行,13例(39.4%)在国际进行。33例ct中,19例(57.6%)被停职,9例(27.3%)被终止,5例(15.2%)被撤销。总体而言,试验中断最常见的原因是招聘困难(24.2%)。因COVID-19而中断的试验中位入组人数为37人(四分位数间距[IQR], 19-71),因其他原因而中断的试验中位入组人数为6人(四分位数间距[IQR], 0-27), Mann-Whitney检验显示两者之间存在统计学差异(z= - 3.913, p<0.001)。试验地点、资金来源、随机分组或研究是否涉及蒙面受试者与未蒙面受试者之间没有显著关联。结论新冠肺炎疫情对耳鼻喉科临床研究产生了影响。为了在未来对参与者互动和沟通的威胁中保持试验的继续,我们建议进一步探索远程监测实践和虚拟程序——这些将保持建立新疗法所需的有效性和准确性。我们鼓励未来的试验来衡量哪些远程评估显示出最大的有效性,其长期目标是建立能够抵御未来流行病的创新研究设计。
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The impact of COVID-19 on otolaryngology research: a cross-sectional analysis of discontinued trials
Abstract Context The COVID-19 pandemic has reduced the capacity to conduct medical research due to recruitment difficulties, supply chain shortages, and funding deficits. The clinical practice of otolaryngology was especially impacted due to a reduction in elective procedures, such as facial plastic surgeries and vocal fold injections. Objectives The primary objective was to examine the extent of clinical trial (CTs) disruption secondary to the COVID-19 pandemic in the field of otolaryngology. Methods On August 1, 2021, we conducted a systematic search utilizing ClinicalTrials.gov for CTs related to common otolaryngology disorders. We utilized the date range January 1, 2020 through August 1, 2021 to identify all trials potentially affected by the COVID-19 pandemic. Investigators performed screening and data extraction in a duplicate, masked fashion. Trials resulting from the search were extracted for trial status, condition treated, enrollment number, funding, study type, study design, last update posted date, and trial location. Trials that explicitly mentioned COVID-19 as a reason for discontinuation or suspension were coded as such. For trials that did not explicitly mention COVID-19, we coded the reason provided from ClinicalTrials.gov. The Oklahoma State University Center for Health Science Institutional Review Board determined that this project did not qualify as human subject research. Results A total of 1,777 CTs met the inclusion criteria, and 223 CTs were discontinued between January 1, 2020 and August 1, 2021. Thirty-three (14.8%) of the 223 CTs reported discontinuation explicitly due to the COVID-19 pandemic. The 33 studies had 1,715 participants enrolled in total. Among the primary interventions, 11 (33.3%) were devices, 10 (30.3%) were drugs, 5 (15.2%) were behavioral, 4 (12.1%) were diagnostic tests, 1 (3.0%) was dietary, and 2 (6.1%) were labeled as “other.” Regarding the CT location, 20 (60.6%) were conducted in the United States, and 13 (39.4%) were conducted internationally. Of the 33 CTs, 19 (57.6%) were suspended, 9 (27.3%) were terminated, and 5 (15.2%) were withdrawn. The overall most common reason for trial disruption was recruitment difficulties (24.2%). Median enrollment for discontinued trials due to COVID-19 was 37 (interquartile range [IQR], 19–71) and for other reasons was 6 (IQR, 0–27), for which the Mann–Whitney test showed a statistically significant difference between the two (z=−3.913, p<0.001). There were no significant associations between trial location, funding source, randomization, or whether a study involved masked vs unmasked participants. Conclusions The COVID-19 pandemic has incited an impact on clinical research in the field of otolaryngology. To preserve trial continuation amid future threats to participant interaction and communication, we recommend further exploration of remote monitoring practices and virtual procedures—those that will maintain the effectiveness and accuracy needed to establish novel therapeutics. We encourage future trials to gauge which remote assessments show the greatest validity, with the long-term goal of establishing innovative study designs resilient to future pandemics.
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