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一项3b期前瞻性随机开放标签盲终点多中心试验的原理与设计,该试验旨在比较尿激酶溶栓与抗血小板药物对轻度中风患者的疗效和安全性。

Rationale and design of a phase 3b, prospective, randomized, open label, blinded-endpoint, multicenter trial of the efficacy and safety of urokinase thrombolysis comparing with antiplatelet agents for patients with minor stroke.

作者信息

Zhao Lu, Jiang Chenyang, Tao Yongli, Gao Yuan, Xu Yafang, Zhang Rui, Liu Kai, Gu Hongqiu, Wang Yilong, Xu Yuming, Song Bo

机构信息

Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, Henan 450052, China.

China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

出版信息

Int J Stroke. 2022 Apr;17(4):474-477. doi: 10.1177/17474930211014344. Epub 2021 May 21.

Abstract

RATIONALE

Minor ischemic stroke attack has taken a significant part of cerebrovascular disease burden. Benefits of thrombolysis in minor stroke is under debates and the use of urokinase in developing countries needs to be further explored.

AIM

TRUST (ThRombolysis of Urokinase for minor STroke) trial was designed to evaluate the efficacy and safety of intravenous urokinase for the treatment of acute minor ischemic stroke.

SAMPLE SIZE ESTIMATES

To reach a double-sided type I error rate of 0.05 to test our hypothesis, with β = 0.80, sample size of 1002 subjects were determined after further adjustment to account for up to 5% nonadherence.

METHODS AND DESIGN

TRUST trial was developed with PROBE design, as a multicenter, randomized, open label, single-blind clinical trial with the stage of phase 3b.

STUDY OUTCOMES

The proportion of patients retaining full ability of independent living, which is defined as patients scoring 0-1 on modified Rankin Scale score at 90 days.

DISCUSSION

TRUST trial may potentially provide promising and affordable thrombolysis for acute minor ischemic stroke in the developing parts of the world.

摘要

理论依据

轻度缺血性中风发作在脑血管疾病负担中占很大一部分。轻度中风溶栓治疗的益处存在争议,在发展中国家尿激酶的使用需要进一步探索。

目的

TRUST(轻度中风尿激酶溶栓)试验旨在评估静脉注射尿激酶治疗急性轻度缺血性中风的疗效和安全性。

样本量估计

为达到双侧I型错误率0.05以检验我们的假设,β = 0.80,在进一步调整以考虑高达5%的不依从性后,确定样本量为1002名受试者。

方法与设计

TRUST试验采用PROBE设计,是一项多中心、随机、开放标签、单盲的3b期临床试验。

研究结果

保持完全独立生活能力的患者比例,定义为90天时改良Rankin量表评分为0 - 1分的患者。

讨论

TRUST试验可能为世界上发展中地区的急性轻度缺血性中风提供有前景且经济实惠的溶栓治疗。

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