首页> 外文OA文献 >Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia
【2h】

Rationale and Design of Randomized Clinical Trial for the Assessment of Macitentan Efficiency as Coadjuvant Treatment to Open and Endovascular Revascularization in Critical Limb Ischemia

机译:用于评估ChiCentan效率作为Coadjuvant治疗在关键肢体缺血中的辅助治疗中的随机临床试验的理由与设计

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Introduction Critical limb ischemia (CLI) is defined by ischemic rest pain, tissue loss, or both, secondary to arterial insufficiency, and its prevalence is increasing mainly as a result of the worldwide high prevalence of diabetes. Currently, there are no available conclusive data on the efficacy of any coadjuvant therapy after revascularization procedure benefiting amputation and patency rates. Macitentan is an orally active dual endothelin (ET) receptor antagonist that may contribute to reduce the amputation rate and improve revascularization patency in CLI. Methods/Design REVASC is a proposed pilot, open-label, controlled, randomized, single-center clinical double-blind trial to be conducted in Spain on a study population of European patients with CLI, which will compare the clinical outcomes and cost-effectiveness of macitentan coadjuvant treatment after limb revascularization with the standard antiplatelet treatment strategy for severe limb ischemia. Patients are randomized 1:1 to receive macitentan or placebo for 12 weeks. The primary clinical end point will be amputation-free survival rate at 12 months, defined as the time to major (above the ankle) amputation for the index (trial) limb or death from any cause, whichever comes first. Secondary outcomes include overall survival, quality of life, in-hospital mortality and morbidity, repeat interventions, healing of tissue loss, and hemodynamic changes following revascularization. Sample size is estimated as 120 patients. The economic analysis will consist of two components: a “within-study” analysis, which will be based on study end points; and a “model-based” analysis, which will extrapolate and compare costs and effects likely to accrue beyond the study follow-up period. Discussion The REVASC trial is designed to be pragmatic and represents current practice of the real-world population management after limb revascularization for CLI due to atherosclerosis. Current evidence does not support any coadjuvant treatment. A new pathway of treatment may be opened with the use of ET receptor antagonists in these patients.
机译:引入严重肢体缺血(CLI)是由缺血性休息痛,组织损失,或两者,继发于动脉供血不足所定义,并且其发病率主要增加糖尿病在世界范围内的高患病率的结果。目前,有任何辅助剂治疗的疗效没有可用的确凿数据血运重建手术后受益截肢和通畅率。美西特田是一种口服有效的双重内皮素(ET)受体拮抗剂,其可以有助于降低截肢率,提高血管再生通畅CLI。方法/设计REVASC被提议的试点,开放标签,对照,随机,单中心临床双盲试验将在西班牙对欧洲病人CLI的研究人群中进行的,这会比较临床疗效和成本效益与严重肢体缺血的标准抗血小板治疗策略肢体血运重建后马西辅助治疗。患者1:1随机接受美西特田或安慰剂治疗12周。主要临床终点将在12个月无截肢生存率,定义为时间主要截肢用于由任何原因引起,以先到者为准的索引(试)肢体或死亡(在踝关节以上)。次要终点包括总生存,生活,住院死亡率和发病率,重复干预质量,组织损失的愈合,血管再通之后血流动力学变化。样本量估计为120个例。经济分析会包括两个组成部分:一个“中学习”的分析,这将是基于研究终点;和“基于模型的”分析,这将推断和可能比较成本和效果,超出了研究随访期起租。讨论的REVASC试验的目的是务实的,并代表肢体血运重建的CLI后的真实世界人口管理的现行做法,由于动脉粥样硬化。目前的证据不支持任何辅助治疗。一种新的治疗途径可能与这些患者使用ET受体拮抗剂被打开。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号