Protocol for a prospective 1-year follow-up investigation on normobaric hyperoxia in conjunction with endovascular treatment for acute ischemic stroke (OPENS-2L) trial.

IF 4.8 4区 医学 Q3 CLINICAL NEUROLOGY
Brain Circulation Pub Date : 2025-03-31 eCollection Date: 2025-04-01 DOI:10.4103/bc.bc_29_24
Ming Wei, Xing Wang, Sifei Wang, Shuling Liu, Xunming Ji, Weili Li
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引用次数: 0

Abstract

Introduction: Ongoing research endeavors seek to identify neuroprotective drugs capable of mitigating brain cell necrosis and reperfusion injury by protecting the ischemic penumbra. Despite these efforts, the quest for effective neuroprotective agents remains elusive. Encouragingly, preliminary investigations, including basic experiments and single-center exploratory studies, have demonstrated the neuroprotective properties of normobaric hyperoxia (NBO). In pursuit of validating and expanding upon these findings, we have conducted a multicenter, prospective, randomized, controlled clinical trial known as OPENS-2. However, the OPENS-2 study only assessed outcomes at a 90-day endpoint, leaving uncertainties regarding the potential long-term benefits of NBO in stroke management. Thus, to address this gap in knowledge, we will initiate a long-term follow-up trial, OPENS-2L, building upon the foundation laid by the OPENS-2 study.

Materials and methods: This prospective, randomized controlled clinical trial will enroll 280 patients at a 1:1 ratio. Patients will be randomly divided into the NBO combined with the endovascular treatment group, where they will receive 10 L/min of oxygen through a mask, or the control group, where they will receive 1 L/min of oxygen.

Results: The primary endpoint of this study is the modified Rankin Scale (mRS) score at 1 year. Secondary endpoints include mRS 0-2, mRS 0-3, mRS 0-1 scores, Barthel index, and the EuroQol-5 Dimension score at 1 year. Safety endpoints encompass all-cause mortality at 1 year and the incidence of major vascular events.

Conclusion: If this trial yields positive outcomes, it would furnish crucial evidence for guiding future neuroprotective research endeavors. Overall, the insights gained from this study hold the potential to illuminate the long-term benefits of NBO combined with endovascular treatment in improving stroke outcomes, thereby shaping the landscape of stroke management practices.

Trial registration: ClinicalTrials.gov NCT05039697.

常压高氧联合血管内治疗急性缺血性卒中的前瞻性1年随访研究方案(open - 2l)试验。
导论:正在进行的研究正在寻找能够通过保护缺血半暗带来减轻脑细胞坏死和再灌注损伤的神经保护药物。尽管有这些努力,寻找有效的神经保护剂仍然难以捉摸。令人鼓舞的是,包括基础实验和单中心探索性研究在内的初步研究已经证明了常压高氧(NBO)的神经保护特性。为了验证和扩展这些发现,我们进行了一项多中心、前瞻性、随机、对照临床试验,称为open -2。然而,open -2研究仅评估了90天终点的结果,对NBO在卒中管理中的潜在长期益处留下了不确定性。因此,为了解决这方面的知识差距,我们将在open -2研究奠定的基础上,启动一项长期的后续试验,open - 2l。材料和方法:本前瞻性、随机对照临床试验将以1:1的比例招募280例患者。患者将被随机分为NBO联合血管内治疗组,通过面罩给氧10l /min,对照组给氧1l /min。结果:本研究的主要终点是1年时的改良Rankin量表(mRS)评分。次要终点包括mRS 0-2、mRS 0-3、mRS 0-1评分、Barthel指数和1年时的EuroQol-5维度评分。安全性终点包括1年内的全因死亡率和主要血管事件的发生率。结论:如果该试验取得积极成果,将为指导未来神经保护研究提供重要证据。总的来说,从这项研究中获得的见解有可能阐明NBO联合血管内治疗在改善卒中预后方面的长期益处,从而塑造卒中管理实践的前景。试验注册:ClinicalTrials.gov NCT05039697。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brain Circulation
Brain Circulation Multiple-
自引率
5.30%
发文量
31
审稿时长
16 weeks
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