跳至主要内容
临床试验/NCT00498940
NCT00498940终止不适用

Biventricular Pacing After Cardiopulmonary Bypass

Henry M. Spotnitz1 个研究点 分布在 1 个国家目标入组 111 人开始时间: 2006年10月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
111
试验地点
1
主要终点
Thermal Dilution Cardiac Index (CI) Measured in the Intensive Care Unit (ICU).

研究概览

简要总结

The purpose of this study is to investigate the efficacy of optimized temporary biventricular pacing (BiVP) in patients undergoing open-heart surgery with preoperative LV dysfunction and an intraventricular conduction delay. This study will compare extended temporary biventricular pacing versus standard of care by assessing patients randomized to the two groups, from the conclusion of cardiopulmonary bypass, until the conclusion of pharmacologic circulatory support in the intensive care unit. In addition, effects of biventricular pacing will be tested in all patients, at three time points, using different measures of blood flow. Results from this research will demonstrate whether temporary BiVP improves cardiac output after open-heart surgery and whether ventricular pacing optimization increases cardiac output in this setting. Success would lead to the development of recommendations for use of BiVP postoperatively and would stimulate the development of pacemakers with appropriate features.

The primary hypothesis is that the optimum pacing protocol (POPT) will increase cardiac index (CI) by 15% (from approximately 2.30 to 2.64 L/min/m2) compared to standard of care as measured by thermodilution 12-24 hours postoperatively. Secondary objectives include defining POPT at three time points within 24 hours of surgery. The investigator will examine which forms of cardiac dysfunction benefit from temporary pacing using direct and indirect measures of perfusion and cardiac function. The investigator will also analyze survival, length of stay, incidence of arrhythmias, and cost of postoperative care.

详细描述

Biventricular pacing (BiVP) reverses intraventricular conduction delay (IVCD) and left ventricular (LV) dysfunction in dilated cardiomyopathy (DCM). BiVP improves LV function and cardiac index (Cl) at no energy cost. In the MIRACLE trial, in patients with DCM, IVCD and LV ejection fraction <35%, demonstrated improved subjective and objective measures of exercise tolerance and cardiac function with BiVP. BiVP benefits many, but selection criteria are not fully developed, and 30% of recipients are "nonresponders," at a cost of more than $2 billion/year. Preliminary data suggest that BiVP can benefit patients with low output states after cardiac surgery. This study will assess surgical application of BiVP while assessing mechanisms of action and optimization. 190 cardiac surgery patients will be randomized with LV dysfunction preoperatively to paced and standard of care groups. BiVP will be optimized and continued postoperatively until patients are stable. BiVP will be assessed transiently in all patients at three time points. The primary end point is a 15% improvement in thermal dilution Cl measured in the intensive care unit (ICU). Effects of heart rate, atrioventricular delay, ventricular pacing site, and interventricular delay on Cl will be assessed using a randomized sequence of data collection. Secondary endpoints include incidence of arrhythmias, inotropic support, urine output, weight gain, morbidity, mortality, and ICU costs. These studies are important because of a high probability of clinical benefit. The methods employed will provide precision, breadth of measurement, and range of pacing sites superior to any other setting. The protocol will provide new and important scientific information that will benefit not only surgical patients but also the general population of BiVP recipients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • LV ejection fraction < 41%
  • QRS duration > 99 msec
  • Mitral and Aortic Valve Repair or Replacement

排除标准

  • Congenital Heart Disease
  • Intracardiac Shunts
  • Preoperative Pacing for Heart Block (2nd or 3rd degree) or Sinus Bradycardia
  • Heart Rate > 120 beats per min after Cardiopulmonary Bypass
  • Preoperative Atrial Fibrillation
  • Previous Cardiac Surgery
  • Inability to undergo biventricular pacing prior to randomization

研究组 & 干预措施

Biventricular Pacing

Active Comparator

After weaning from bypass, patients received temporary biventricular pacing for 24 hours. Values obtained from optimization testing determined pacemaker settings (AVD, VVD, heart rate).

干预措施: Optimization Testing (Device)

Biventricular Pacing

Active Comparator

After weaning from bypass, patients received temporary biventricular pacing for 24 hours. Values obtained from optimization testing determined pacemaker settings (AVD, VVD, heart rate).

干预措施: Temporary Biventricular Pacing (Device)

Standard of Care

Active Comparator

No continuous pacing occurred about surgery. Patients underwent optimization testing.

干预措施: Optimization Testing (Device)

结局指标

主要结局

Thermal Dilution Cardiac Index (CI) Measured in the Intensive Care Unit (ICU).

时间窗: 24 hours

Cardiac output (CO) 12-24 hours after bypass is measured five times and averaged. CO is then converted to CI, after division by the patient's body surface area.

次要结局

  • Number of Subjects With Postoperative Complications(30 days after surgery)

研究者

发起方
Henry M. Spotnitz
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Henry M. Spotnitz

George H. Humphreys, II Professor of Surgery

Columbia University

研究点 (1)

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