跳至主要内容
临床试验/NCT02512731
NCT02512731已完成不适用

Intraoperative Fluid Therapy for Deceased Donor Renal Transplantation

University Health Network, Toronto2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2012年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
The volume of crystalloid solutions administered intraoperatively.

研究概览

简要总结

Delayed graft function (DGF) is defined as requirement for dialysis in the first week following kidney transplantation. DGF is a common complication occurring in 39% of the deceased donor renal transplants at the investigators' institution with significant cost and outcome implications. The 3 major risk factors for DGF are donor graft characteristics, recipient factors and perioperative management. The most easily modifiable of these factors is perioperative management, in particular intraoperative fluid therapy. The investigators propose to compare the amount of fluid administered using the current standard of care with the fluid administered when optimizing the cardiac output (CO) using Esophageal Doppler Monitoring (EDM) to guide fluid therapy. EDM measures blood flow in the descending aorta, optimizing stroke volume (SV) and cardiac output (CO) by indicating when fluid administration fails to produce an increase in CO.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Prevention
盲法
Single (Outcomes Assessor)

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

  • age greater than 18 years
  • signed informed consent
  • listed for deceased donor transplantation.

排除标准

  • esophageal surgery or cancer
  • esophageal stricture, varices or diverticulum
  • upper airway surgery
  • coarctation of the aorta
  • significant valvular heart disease
  • clinically significant cardiac arrhythmias
  • patient randomized to other trials with an outcome variable of delayed graft function or early graft function will also be excluded

结局指标

主要结局

The volume of crystalloid solutions administered intraoperatively.

时间窗: Start of Anesthesia until the doppler is removed at the end of surgery, approximately 8 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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