Efficacy and safety of ozone therapy administered by autologous blood transfusion for acute ischemic stroke: study protocol for a multi-center open-label large-sample parallel randomized controlled trial

Jing Qiu, Huisheng Chen
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引用次数: 3

Abstract

Background: There is still a lack of effective treatments for acute ischemic stroke. Our pre-clinical studies suggest that ozone therapy administered by autologous blood transfusion is a convenient and safe treatment for ischemic stroke, and is popular with patients, but its therapeutic benefits are not clear. We hypothesized that ozone therapy administered by autologous blood transfusion for ischemic stroke is safe and effective, and propose a protocol for a prospective, multi-center, open-label, large-sample, parallel, randomized, non-blinded controlled trial. Methods/Design: This will be a multi-center, open-label, large-sample, parallel, randomized controlled trial. We intend to recruit 5,000 patients with acute ischemic stroke in 30 centers (including General Hospital of Shenyang Military Region, China). Patients will be randomly allocated to a control group (n = 2,500; conventional stroke therapy) or an ozone therapy group (n = 2,500; ozone therapy administered in addition to conventional therapy). The primary outcome will be a modified Rankin Scale score 0-2 at 90 days. Secondary outcomes will be National Institute of Health Stroke Scale score at 14 days, blood lipid and glucose concentrations and coagulation function at 14 days, and the incidence of post-stroke pneumonia, recurrent stroke and other vascular events in the first 90 days after stroke. Discussion: We hope that our results will illuminate the therapeutic benefits of ozone therapy administered by autologous blood transfusion for acute ischemic stroke. Trial registration: This trial was registered at Chinese Clinical Trial Registry (registration No. ChiCTR-ICR-15007093) on 18 September 2015.
自体输血臭氧治疗急性缺血性卒中的疗效和安全性:一项多中心开放标签大样本平行随机对照试验的研究方案
背景:急性缺血性脑卒中的有效治疗方法尚缺乏。我们的临床前研究表明,自体输血臭氧治疗是一种方便、安全的缺血性卒中治疗方法,受到患者的欢迎,但其治疗效果尚不清楚。我们假设自体输血臭氧治疗缺血性脑卒中是安全有效的,并提出了一项前瞻性、多中心、开放标签、大样本、平行、随机、非盲法对照试验方案。方法/设计:这将是一项多中心、开放标签、大样本、平行、随机对照试验。我们拟招募30个中心(包括中国沈阳军区总医院)的5000例急性缺血性脑卒中患者。患者将被随机分配到对照组(n = 2,500;常规脑卒中治疗组)或臭氧治疗组(n = 2,500;在常规治疗的基础上进行臭氧治疗)。主要结果将是90天的修正兰金量表评分0-2分。次要结局将是14天的美国国立卫生研究院卒中量表评分,14天的血脂和血糖浓度和凝血功能,以及卒中后90天内卒中后肺炎、复发性卒中和其他血管事件的发生率。讨论:我们希望我们的结果将阐明自体输血臭氧治疗急性缺血性脑卒中的疗效。试验注册:本试验在中国临床试验注册中心注册(注册号:ChiCTR-ICR-15007093)于2015年9月18日发布。
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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