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The Danish On-pump, Off-pump Randomization Study (DOORS)

2013年11月5日 更新者:Kim Houlind

The Impact of Avoiding Cardiopulmonary By-pass During Coronary Artery Bypass Surgery for Ischemic Heart Disease in Elderly Patients: The Danish On-pump, Off-pump Randomization Study (DOORS)

Background: Coronary artery bypass grafting (CABG) can be performed either with or without the use of cardiopulmonary bypass (CPB) to obtain myocardial re-vascularisation. The investigators hypothesize that CABG without the use of CPB may reduce the risk of perioperative death, stroke, myocardial infarction and other serious complications.

The aim of the present study is to compare the incidence of complications and the clinical efficacy of CABG with and without the use of CPB in elderly patients.

研究概览

详细说明

Conventional coronary artery bypass grafting (CCABG) using cardiopulmonary bypass has for decades been applied to obtain myocardial re-vascularisation and, hence, improved quality of life and survival. It does, however, bear a risk of death, stroke, myocardial infarction and other serious complications.

During recent years, an equivalent operation performed on the beating heart without cardiopulmonary bypass (off-pump coronary artery bypass grafting, OPCAB) has gained popularity helped by the advent of mechanical stabilization devices and improved surgical techniques. Observational studies suggest that this technique is associated with a lower incidence of stroke, per operative arrhythmias and even mortality than conventional CCABG. This is especially the case in elderly patients and patients with significant co-morbidity.

Only few randomised, controlled trials have been conducted and most of these included mainly or only low-risk, relatively young patients. These studies have documented the safety and efficacy of OPCAB compared with CCABG, but none of the trials has had the statistical strength to determine whether the rate of serious complications is lower after OPCAB operations. One recent study found graft patency to be significantly lower after OPCAB than after CCABG operations.

The investigators find that there is a need of a larger scale randomised trial to compare the results of CCABG and OPCAB operations, especially in elderly patients. This patient group is poorly represented in earlier randomised trials, whereas observational studies and theoretical considerations imply that they may benefit the most from avoiding cardiopulmonary bypass.

Aims: Primarily, to compare the incidence of death, stroke and myocardial infarction after CCABG and OPCAB procedures in a population of elderly patients. Furthermore, to compare quality of life and graft patency, and cost- effectiveness after CCABG and OPCAB.

研究类型

介入性

注册 (实际的)

900

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Aarhus、丹麦、8200
        • Dept. of Cardiothoracic and Vascular Surgery, Skejby Sygehus, Aarhus University Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

70年 及以上 (年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Age seventy years or above
  • Admitted for first time coronary artery bypass operation

Exclusion Criteria:

  • Given information cannot be understood
  • Aortic crossclamping not safe due to calcification
  • Preoperative cardiac conditions demanding cardiopulmonary bypass
  • Re-do cardiac surgery
  • Patients requiring operation within the same day after conference

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:CCABG
Coronary artery bypass surgery using cardiopulmonary bypass
实验性的:OPCAB
Coronary artery bypass surgery NOT using cardiopulmonary bypass

研究衡量的是什么?

主要结果指标

结果测量
大体时间
A combined endpoint of death + stroke + myocardial infarction within 30 days from operation
大体时间:30 days
30 days

次要结果测量

结果测量
大体时间
A combined endpoint of death + stroke + myocardial infarction during follow-up
大体时间:3 years
3 years
Patency of bypass grafts assessed by coronary angiography 6 months after the operation
大体时间:6 months
6 months
Total mortality and cardiac mortality during follow-up
大体时间:3 years
3 years
Need of new intervention for cardiac angina during follow-up
大体时间:3 years
3 years
Quality of life assessed by MOS SF-36 and EuroQol questionnaires 6 months and 3 years after the operation
大体时间:6 months and 3 years
6 months and 3 years
Total hospital costs and costs of public care provided 6 months and 3 years after the operation and difference in costs per quality adjusted life year
大体时间:6 months and 3 years
6 months and 3 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

调查人员

  • 首席研究员:Kim C Houlind, MD, PhD、Aarhus University Hospital
  • 学习椅:Poul E Mortensen, MD、Odense University Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2005年1月1日

初级完成 (实际的)

2008年11月1日

研究完成 (实际的)

2011年1月1日

研究注册日期

首次提交

2005年7月25日

首先提交符合 QC 标准的

2005年7月25日

首次发布 (估计)

2005年7月26日

研究记录更新

最后更新发布 (估计)

2013年11月6日

上次提交的符合 QC 标准的更新

2013年11月5日

最后验证

2013年11月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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