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临床试验/NCT00928460
NCT00928460撤回不适用

The Efficacy of Routine Preoperative Electrocardiography in Patients Undergoing Non-cardiac Surgery

UMC Utrecht1 个研究点 分布在 1 个国家开始时间: 2009年6月26日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
UMC Utrecht
试验地点
1
主要终点
Cardiac death or perioperative myocardial infarction

研究概览

简要总结

A preoperative electrocardiogram (ECG) is nearly routinely performed by anesthesiologists in elderly non-cardiac surgery patients as part of pre-anesthesia evaluation. However, the added value of this routine ECG beyond patient history and physical examination is questionable. The ECGtrial will investigate the efficacy of routine preoperative electrocardiography in patients undergoing non-cardiac surgery.

详细描述

Objective:

A routine ECG is performed as part of the standard diagnostic workup before non-cardiac surgery. However, the added value of this test beyond patient history and physical examination is questionable. The proposed study therefore aims to determine whether preoperative assessment without ECG is more cost-effective.

Study design:

Prospective stepped wedge design multicenter trial including 40,000 patients.

Study population:

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients aged 60 years or older scheduled for noncardiac surgery with an expected hospital length of stay of at least 2 days
  • Patients aged under 60 years but with risk factors for cardiovascular disease scheduled for noncardiac surgery with an expected hospital length of stay of at least 2 days

排除标准

  • Patients refusing informed consent for obtaining blood samples (troponin measurement) at the first two days after surgery
  • Patients refusing participation in long-term clinical and Quality of Life measurements

结局指标

主要结局

Cardiac death or perioperative myocardial infarction

时间窗: 2 days postoperatively

次要结局

  • Other major cardiovascular complications(2 days postoperatively)
  • Death from other causes(2 days postoperatively)
  • Long term quality of life(One year)

研究者

发起方
UMC Utrecht
申办方类型
Other
责任方
Principal Investigator
主要研究者

Wilton A van Klei

MD PhD

UMC Utrecht

研究点 (1)

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