Department of Neurology and Rehabilitation Medicine, University of Cincinnati Gardner Neuroscience Institute, OH (J.P.B., Y.A., E.A.M.).
Federal University of São Paulo, Clinical Trialist/Neurology, Albert Einstein Hospital, São Paulo, Brazil (G.S.S.).
Stroke. 2023 Oct;54(10):2698-2707. doi: 10.1161/STROKEAHA.123.044149. Epub 2023 Sep 11.
The Stroke Treatment Academic Industry Roundtable (STAIR) convened a session and workshop regarding enrollment in acute stroke trials during the STAIR XII meeting on March 22, 2023. This forum brought together stroke physicians and researchers, members of the National Institute of Neurological Disorders and Stroke, industry representatives, and members of the US Food and Drug Administration to discuss the current status and opportunities for improving enrollment in acute stroke trials. The workshop identified the most relevant issues impacting enrollment in acute stroke trials and addressed potential action items for each. Focus areas included emergency consent in the United States and other countries; careful consideration of eligibility criteria to maximize enrollment and representativeness; investigator, study coordinator, and pharmacist availability outside of business hours; trial enthusiasm/equipoise; site start-up including contractual issues; site champions; incorporation of study procedures into standard workflow as much as possible; centralized enrollment at remote sites by study teams using telemedicine; global trials; and coenrollment in trials when feasible. In conclusion, enrollment of participants is the lifeblood of acute stroke trials and is the rate-limiting step for testing an exciting array of new approaches to improve patient outcomes. In particular, efforts should be undertaken to broaden the medical community's understanding and implementation of emergency consent procedures and to adopt designs and processes that are easily incorporated into standard workflow and that improve trials' efficiencies and execution. Research and actions to improve enrollment in ongoing and future trials will improve stroke outcomes more broadly than any single therapy under consideration.
中风治疗学术产业圆桌会议(STAIR)于 2023 年 3 月 22 日在第 12 届 STAIR 会议期间召开了一次关于急性中风试验入组的会议和研讨会。该论坛汇集了中风医生和研究人员、美国国立神经病学与中风研究所的成员、行业代表以及美国食品和药物管理局的成员,讨论了急性中风试验入组的现状和机会。研讨会确定了影响急性中风试验入组的最相关问题,并针对每个问题提出了潜在的行动方案。重点领域包括美国和其他国家的紧急同意;仔细考虑资格标准,以最大限度地增加入组人数和代表性;调查员、研究协调员和药剂师在工作时间外的可用性;试验积极性/平衡;试验启动包括合同问题;试验负责人;尽可能将研究程序纳入标准工作流程;研究团队通过远程医疗在远程站点集中入组;全球试验;以及在可行的情况下共同参与试验。总之,参与者的入组是急性中风试验的生命线,也是测试一系列新方法以改善患者结局的限速步骤。特别是,应该努力扩大医学界对紧急同意程序的理解和实施,并采用易于纳入标准工作流程且提高试验效率和执行的设计和流程。为改善正在进行和未来试验的入组而进行的研究和行动将比任何正在考虑的单一疗法更广泛地改善中风结局。