The George Institute for Global Health China, Beijing, China.
The George Institute for Global Health, Faculty of Medicine, The University of New South Wales (UNSW), Sydney, NSW, Australia.
Int J Stroke. 2023 Mar;18(3):364-369. doi: 10.1177/17474930221120345. Epub 2022 Aug 24.
Uncertainty exists over the optimal level of blood pressure (BP) after mechanical thrombectomy (MT) for acute ischemic stroke (AIS).
We aim to determine the effectiveness and safety of intensive BP-lowering following MT reperfusion of large-vessel occlusion (LVO)-related AIS.
The second ENhanced Control of Hypertension ANd Thrombolysis strokE stuDy (ENCHANTED2) is an investigator-initiated, multicenter, prospective, randomized, open, blinded-endpoint (PROBE) trial of intensive systolic BP (SBP) control in reperfused (extended treatment in cerebral infarction (eTICI) classification 2b/2c/3) LVO-AIS patients with persistent hypertension (SBP ⩾ 140 mmHg) at 60+ sites in China, and Australia and the United Kingdom. Eligible patients are centrally randomly allocated to more- (target SBP ⩽ 120 mmHg within 1 h) or less-intensive (target SBP 140-180 mmHg) BP management, to be maintained for 72 h. Primary outcome is an ordinal shift analysis of scores on the modified Rankin scale (mRS) at 90 days. Sample size of 2257 patients provides 90% power to detect a 6.5% absolute reduction in poor outcome from more-intensive BP-lowering using ordinal logistic regression.
Recruitment started in China in July 2020. At a meeting of the independent Data and Safety Monitoring Board in March 2022 to review primary outcome data available for 347 patients, they recommended suspension of recruitment due to safety concerns in the more-intensive group; which was implemented by the Trial Steering Committee (TSC) with 817 randomized patients only in China. The TSC then stopped recruitment after the safety concerns persisted on further review of the data in June 2022. The TSC will make a decision on restarting the trial with modification of the protocol when the results are made public.
ENCHANTED2 will provide further randomized evidence on the role of intensive BP-lowering after reperfusion in MT-treated AIS patients.
ClinicalTrials.gov NCT04140110; registered 25 October 2019.
机械取栓(MT)后血压(BP)的最佳水平尚不确定,特别是对于急性缺血性脑卒中(AIS)患者。
我们旨在确定大血管闭塞(LVO)相关 AIS 再灌注后强化降压的有效性和安全性。
第二项强化降压和溶栓治疗对卒中影响研究(ENCHANTED2)是一项由研究者发起的、多中心、前瞻性、随机、开放、盲终点(PROBE)试验,旨在评估强化收缩压(SBP)控制对伴有持续性高血压(SBP≥140mmHg)的 LVO-AIS 患者(脑梗死再灌注扩展治疗分类 2b/2c/3)的影响。在中国、澳大利亚和英国的 60 多个中心,对符合条件的患者进行中心随机分配,接受更强化(目标 SBP≤120mmHg,1h 内)或更不强化(目标 SBP 140-180mmHg)的降压管理,持续 72h。主要结局是 90 天时改良 Rankin 量表(mRS)评分的有序转移分析。2257 例患者的样本量为 90%,可通过有序逻辑回归检测更强化降压治疗降低不良结局的 6.5%绝对风险。
该研究于 2020 年 7 月在中国开始招募。在 2022 年 3 月由独立的数据和安全监测委员会召开的会议上,对 347 例患者的主要结局数据进行了审查,由于更强化组的安全性问题,他们建议暂停招募,该建议得到了试验指导委员会(TSC)的执行,仅在中国有 817 例随机患者参与了该研究。随后,在 2022 年 6 月进一步审查数据后,当安全性问题持续存在时,TSC 停止了招募。当结果公布时,TSC 将根据方案修改决定是否重新启动试验。
ENCHANTED2 将为 MT 治疗的 AIS 患者再灌注后强化降压的作用提供更多的随机证据。
ClinicalTrials.gov NCT04140110;于 2019 年 10 月 25 日注册。