急性缺血性卒中(TRICS)远程缺血调节的多中心转化试验:来自意大利卒中组织(ISO)基础科学网络的多中心,平行组,随机,雌性和雄性大鼠和小鼠临床前试验方案。

Q1 Medicine BMJ Open Science Pub Date : 2020-11-24 eCollection Date: 2020-01-01 DOI:10.1136/bmjos-2020-100063
Mauro Tettamanti, Simone Beretta, Giuseppe Pignataro, Stefano Fumagalli, Carlo Perego, Luigi Sironi, Felicita Pedata, Diana Amantea, Marco Bacigaluppi, Antonio Vinciguerra, Alessia Valente, Susanna Diamanti, Jacopo Mariani, Martina Viganò, Francesco Santangelo, Chiara Paola Zoia, Virginia Rogriguez-Menendez, Laura Castiglioni, Joanna Rzemieniec, Ilaria Dettori, Irene Bulli, Elisabetta Coppi, Giorgia Serena Gullotta, Giacinto Bagetta, Gianvito Martino, Carlo Ferrarese, Maria Grazia De Simoni
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引用次数: 6

摘要

多中心临床前随机对照试验(pRCT)正在成为确认疗效和改善临床转化的必要步骤。本项目的目的是进行两个多中心prct(一个在大鼠和一个在小鼠中)来研究远程缺血调节(RIC)在严重缺血性卒中实验模型中的疗效。方法和分析:意大利中风组织(ISO)基础科学网络中的七个研究实验室将参与这项研究。将在两种动物(大鼠和小鼠)和两性中进行右大脑中动脉近端血管内短暂闭塞。动物将被随机分配,在再灌注后通过右股动脉短暂手术闭塞或假手术接受RIC。将对48小时的二分功能神经评分(主要终点)和梗死体积(次要终点)进行盲法结局评估。每个物种80只动物的样本量将产生82%的能力来检测两个prct中30%的主要结果的显著差异。分析将在盲状态下进行,并根据意向治疗范式。这项研究的结果将提供强有力的、面向翻译的、高质量的证据,证明RIC对多种啮齿类动物缺血性卒中的疗效。伦理和传播:这是由米兰比可卡大学动物福利监管机构批准的,并获得意大利卫生部的项目许可。试验结果将根据本方案中提出的结果定义进行公布。试验注册号:PCTE0000177。
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Multicentre translational Trial of Remote Ischaemic Conditioning in Acute Ischaemic Stroke (TRICS): protocol of multicentre, parallel group, randomised, preclinical trial in female and male rat and mouse from the Italian Stroke Organization (ISO) Basic Science network.

Introduction: Multicentre preclinical randomised controlled trials (pRCT) are emerging as a necessary step to confirm efficacy and improve translation into the clinic. The aim of this project is to perform two multicentre pRCTs (one in rats and one in mice) to investigate the efficacy of remote ischaemic conditioning (RIC) in an experimental model of severe ischaemic stroke.

Methods and analysis: Seven research laboratories within the Italian Stroke Organization (ISO) Basic Science network will participate in the study. Transient endovascular occlusion of the proximal right middle cerebral artery will be performed in two species (rats and mice) and in both sexes. Animals will be randomised to receive RIC by transient surgical occlusion of the right femoral artery, or sham surgery, after reperfusion. Blinded outcome assessment will be performed for dichotomised functional neuroscore (primary endpoint) and infarct volume (secondary endpoint) at 48 hours. A sample size of 80 animals per species will yield 82% power to detect a significant difference of 30% in the primary outcome in both pRCTs. Analyses will be performed in a blind status and according to an intention-to-treat paradigm. The results of this study will provide robust, translationally oriented, high-quality evidence on the efficacy of RIC in multiple species of rodents with large ischaemic stroke.

Ethics and dissemination: This is approved by the Animal Welfare Regulatory Body of the University of Milano Bicocca, under project license from the Italian Ministry of Health. Trial results will be subject to publication according to the definition of the outcome presented in this protocol.

Trial registration number: PCTE0000177.

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来源期刊
BMJ Open Science
BMJ Open Science Medicine-General Medicine
CiteScore
10.00
自引率
0.00%
发文量
9
审稿时长
31 weeks
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