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多中心、随机、患者盲法两阶段临床试验:内皮功能试验对非阻塞性冠状动脉疾病患者影响的研究(ENDOFIND)。

Rationale and design of a multicenter, randomized, patients-blinded two-stage clinical trial on effects of endothelial function test in patients with non-obstructive coronary artery disease (ENDOFIND).

机构信息

Vascular Medicine Center, Peking University Shougang Hospital, Beijing, PR China; Vascular Health Research Center of Peking University Health Science Center(VHRC-PKUHSC), Beijing, PR China.

Peking University Clinical Research Institute, Peking University Health Science Center, Beijing, PR China.

出版信息

Int J Cardiol. 2021 Feb 15;325:16-22. doi: 10.1016/j.ijcard.2020.10.033. Epub 2020 Oct 16.

Abstract

Abnormal peripheral and coronary endothelial function has been associated with increased risk of major adverse cardiovascular events (MACE) in cross-sectional retrospective and observational studies. However, prognostic value of routine clinical evaluation, diagnosis and treatment of endothelial dysfunction on incident MACE in patients with non-obstructive coronary artery disease (NOCAD) remains unknown. Endothelial Function Guided Management in Patients with NOCAD (ENDOFIND) is a multicenter, randomized, patients-blinded, parallel-controlled, two-stage clinical trial evaluating the impact of routine clinical peripheral endothelial function testing on initiation and/or intensification of cardiovascular preventive therapies in Stage I, and on the risk of MACE in Stage II in patients with NOCAD. One thousand participants with NOCAD on clinically indicated coronary computed tomography or invasive angiography will be enrolled and randomized 1:1, after baseline peripheral endothelial function evaluation, to either endothelial function guided treatment group or standard of care control group. In Stage I, patients will be followed for 12 months and primary outcome will be the proportion of patients receiving prescriptions for cardiovascular evidence-based lipid, blood pressure and glucose lowering medications at the clinic visit immediately after endothelial function evaluation. Secondary outcomes are change in endothelial function measured as reactive hyperemia index and patients' adherence to evidence-based medications in 12 months. Study will be extended into Stage II where sample size and follow up duration will be reevaluated to ensure statistical power, and primary outcome will be incident MACE. ENDOFIND is proof-of-concept clinical trial of a disruptive endothelial function guided clinical intervention with potential benefits to NOCAD patients. CONDENSED ABSTRACT: ENDOFIND is a proof-of-concept clinical trial of a disruptive endothelial function guided clinical intervention with potential benefits to patients with no obstructive coronary artery disease (NOCAD). It is a multicenter, randomized, patients-blinded, parallel controlled two-stage clinical trial to evaluate the impact of routine clinical peripheral endothelial function testing on initiation and/or intensification of cardiovascular disease preventive therapies in Stage I, and on the risk of MACE in Stage II.

摘要

异常的外周和冠状动脉内皮功能与主要不良心血管事件(MACE)的风险增加有关,这在横断面回顾性和观察性研究中已有报道。然而,在非阻塞性冠状动脉疾病(NOCAD)患者中,常规临床评估、内皮功能障碍的诊断和治疗对首发 MACE 的预后价值尚不清楚。非阻塞性冠状动脉疾病患者内皮功能指导管理(ENDOFIND)是一项多中心、随机、患者设盲、平行对照的两阶段临床试验,旨在评估常规临床外周内皮功能检测对 I 期心血管预防治疗的启动和/或强化,以及对 NOCAD 患者 II 期 MACE 风险的影响。将纳入 1000 名有临床指征的经冠状动脉计算机断层扫描或有创血管造影的 NOCAD 患者,在基线外周内皮功能评估后,按 1:1 随机分为内皮功能指导治疗组或标准治疗对照组。在 I 期,患者将随访 12 个月,主要结局是内皮功能评估后就诊时接受心血管循证调脂、降压和降糖药物处方的患者比例。次要结局是内皮功能的变化,用反应性充血指数来衡量,以及 12 个月内患者对循证药物的依从性。研究将扩展到 II 期,届时将重新评估样本量和随访时间,以确保统计学效力,主要结局是首发 MACE。ENDOFIND 是一项具有颠覆性的内皮功能指导临床干预的概念验证临床试验,可能使 NOCAD 患者受益。

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