Yang Xiang, Shu Yang, Lei Guo, Chongya Dong, Charles B L M Majoie, Adnan H Siddiqui, J Mocco, Fabiano Cavalcante, Bing-Hu Li, Jian-Hong Wang, Bin Huang, Duo-Zi Wang, Neng-Wei Yu, Wouter J Schonewille, Aquilla S Turk, Fu-Qiang Guo
{"title":"BEST-BAO:一项多中心、前瞻性、随机对照试验,研究血管内治疗伴或不伴静脉溶栓治疗基底动脉闭塞性急性缺血性卒中的方案和原理。","authors":"Yang Xiang, Shu Yang, Lei Guo, Chongya Dong, Charles B L M Majoie, Adnan H Siddiqui, J Mocco, Fabiano Cavalcante, Bing-Hu Li, Jian-Hong Wang, Bin Huang, Duo-Zi Wang, Neng-Wei Yu, Wouter J Schonewille, Aquilla S Turk, Fu-Qiang Guo","doi":"10.1136/svn-2025-004144","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Endovascular treatment (EVT) is safe and effective in treating acute ischaemic stroke due to basilar artery occlusion (AIS-BAO); nonetheless, the impact of intravenous thrombolysis (IVT) on its efficacy remains unclear.</p><p><strong>Objective: </strong>To compare the effectiveness and safety of EVT with or without prior IVT in treating AIS-BAO patients within 4.5 hours after stroke onset.</p><p><strong>Methods and design: </strong>A multicentre, prospective, randomised, open-label controlled clinical trial with blinded assessment of endpoints. 340 patients will be consecutively randomised to receive IVT plus EVT or direct EVT in a ratio of 1:1 from about 100 hospitals in China. An interim analysis is planned when one-third (114) of the patients have completed the primary endpoint follow-ups. It anticipates that IVT plus EVT demonstrates superiority over direct EVT. If the superiority of IVT plus EVT over direct EVT is less than expected, the sample size may be expanded by up to 20% of the original size. If the efficacy of the two groups is similar, it will shift to a non-inferiority hypothesis, aiming to evaluate whether direct EVT is non-inferior to IVT plus EVT.</p><p><strong>Outcome: </strong>The primary endpoint is the proportion of independent neurological function defined as a modified Rankin Scale score of 0 to 2 at 90±14 days after stroke onset.</p><p><strong>Discussion: </strong>This trial is expected to provide novel evidence of the superiority or non-inferiority between EVT with or without IVT in the treatment of patients with AIS-BAO.</p><p><strong>Trial registration: </strong>NCT05631847 at ClinicalTrials.gov and ChiCTR2300070584 at Chictr.org.cn.</p>","PeriodicalId":48733,"journal":{"name":"Journal of Investigative Medicine","volume":" ","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"BEST-BAO: a multicentre, prospective, randomised controlled trial of endovascular treatment with or without intravenous thrombolysis in acute ischaemic stroke due to basilar artery occlusion - study protocol and rationale.\",\"authors\":\"Yang Xiang, Shu Yang, Lei Guo, Chongya Dong, Charles B L M Majoie, Adnan H Siddiqui, J Mocco, Fabiano Cavalcante, Bing-Hu Li, Jian-Hong Wang, Bin Huang, Duo-Zi Wang, Neng-Wei Yu, Wouter J Schonewille, Aquilla S Turk, Fu-Qiang Guo\",\"doi\":\"10.1136/svn-2025-004144\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Endovascular treatment (EVT) is safe and effective in treating acute ischaemic stroke due to basilar artery occlusion (AIS-BAO); nonetheless, the impact of intravenous thrombolysis (IVT) on its efficacy remains unclear.</p><p><strong>Objective: </strong>To compare the effectiveness and safety of EVT with or without prior IVT in treating AIS-BAO patients within 4.5 hours after stroke onset.</p><p><strong>Methods and design: </strong>A multicentre, prospective, randomised, open-label controlled clinical trial with blinded assessment of endpoints. 340 patients will be consecutively randomised to receive IVT plus EVT or direct EVT in a ratio of 1:1 from about 100 hospitals in China. An interim analysis is planned when one-third (114) of the patients have completed the primary endpoint follow-ups. It anticipates that IVT plus EVT demonstrates superiority over direct EVT. If the superiority of IVT plus EVT over direct EVT is less than expected, the sample size may be expanded by up to 20% of the original size. 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BEST-BAO: a multicentre, prospective, randomised controlled trial of endovascular treatment with or without intravenous thrombolysis in acute ischaemic stroke due to basilar artery occlusion - study protocol and rationale.
Background: Endovascular treatment (EVT) is safe and effective in treating acute ischaemic stroke due to basilar artery occlusion (AIS-BAO); nonetheless, the impact of intravenous thrombolysis (IVT) on its efficacy remains unclear.
Objective: To compare the effectiveness and safety of EVT with or without prior IVT in treating AIS-BAO patients within 4.5 hours after stroke onset.
Methods and design: A multicentre, prospective, randomised, open-label controlled clinical trial with blinded assessment of endpoints. 340 patients will be consecutively randomised to receive IVT plus EVT or direct EVT in a ratio of 1:1 from about 100 hospitals in China. An interim analysis is planned when one-third (114) of the patients have completed the primary endpoint follow-ups. It anticipates that IVT plus EVT demonstrates superiority over direct EVT. If the superiority of IVT plus EVT over direct EVT is less than expected, the sample size may be expanded by up to 20% of the original size. If the efficacy of the two groups is similar, it will shift to a non-inferiority hypothesis, aiming to evaluate whether direct EVT is non-inferior to IVT plus EVT.
Outcome: The primary endpoint is the proportion of independent neurological function defined as a modified Rankin Scale score of 0 to 2 at 90±14 days after stroke onset.
Discussion: This trial is expected to provide novel evidence of the superiority or non-inferiority between EVT with or without IVT in the treatment of patients with AIS-BAO.
Trial registration: NCT05631847 at ClinicalTrials.gov and ChiCTR2300070584 at Chictr.org.cn.
期刊介绍:
Journal of Investigative Medicine (JIM) is the official publication of the American Federation for Medical Research. The journal is peer-reviewed and publishes high-quality original articles and reviews in the areas of basic, clinical, and translational medical research.
JIM publishes on all topics and specialty areas that are critical to the conduct of the entire spectrum of biomedical research: from the translation of clinical observations at the bedside, to basic and animal research to clinical research and the implementation of innovative medical care.