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临床试验/NCT03673475
NCT03673475已完成不适用

Internal Jugular Vein Distensibility and Pleth Variability Index for Evaluating Fluid Responsiveness

Tepecik Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
number of patients with significant change in VJI distensibility and pleth variebility index

研究概览

简要总结

Assessment of intravascular volume status is crucial in order to predict the efficacy of volume status in major abdominal surgery. The aim of the study is to verify the feasibility and usefulness of the internal jugular vein distensibility index as an adjunct to the pleth variebility index(PVI) to predict fluid responsiveness in major abdominal surgery.

详细描述

Forty patients above age 18 and ASA status I-III who are undergoing major abdominal surgery will be enrolled in the study. patients with right heart failure, arrythmia, severe valve stenosis or regurgitation will be excluded. After induction of general anesthesia, when the patients are hemodynamically stabilised, PVI and jugular vein distensibility will be calculated and recorded. after volume load with 500 ml gel infusion(in 15 min), measurements will be repeated within 10 minutes and recorded. Patients will be allocated to 2 groups according to the change in mean arterial pressure(MAP) after volume expansion: Responders will be defined as an increase in MAP by >%10; while nonresponders will be defined as an increase in MAP <%10 or decrease in MAP.

研究设计

研究类型
Observational
观察模型
Other
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

  • American Society of Anesthesiologists(ASA) physical status I-III patients
  • patients undergoing major abdominal surgery

排除标准

  • arrythmia
  • severe right ventricle failure

结局指标

主要结局

number of patients with significant change in VJI distensibility and pleth variebility index

时间窗: during surgery at day 0

volume responders with significant change in jugular vein distensibility and pleth variebility index

次要结局

未报告次要终点

研究者

发起方
Tepecik Training and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

MELTEM CAKMAK

Anesthesiologist

Tepecik Training and Research Hospital

研究点 (1)

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