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临床试验/NCT03731377
NCT03731377Unknown不适用

The Effectiveness of Mini-fluid Challenge in Predicting Fluid Responsiveness During Video Assisted Thoracic Surgery

National Taiwan University Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年10月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
100
试验地点
1
主要终点
Change of blood pressure after fluid loading

研究概览

简要总结

Perioperative fluid management is crucial for patients' outcome. Muller et al developed a "Mini-fluid challenge method " to predict fluid responsiveness and the efficacy. The investigators design the study to investigate the effectiveness of mini-fluid challenge test in video assisted thoracic surgery.

详细描述

Perioperative fluid management is crucial for patients' outcome. Series of studies have indicated that adequate fluid management optimizes the cardiac out put, improves tissue perfusion, thus decrease the risk of postoperative morbidity. Muller et al developed a "Mini-fluid challenge method " to predict fluid responsiveness and the efficacy. Fluid status and proper perfusion condition in patients undergo thoracic surgery are especially crucial for the vulnerability of lung toward fluid overload. To the best of our knowledge, the efficacy of the test was not discussed in the perioperative care in video assisted thoracic surgery. The investigators design the study to investigate the effectiveness of mini-fluid challenge test in video assisted thoracic surgery.

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
Double (Participant, Care Provider)

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients receiving scheduled video assisted thoracic surgery
  • BMI 18.5~30 kg.m-2

排除标准

  • age younger then 20 yrs or elder than 80 yrs
  • pregnant women
  • patients in intensive care units
  • patients with the underlying disease including respiratory failure(FEV1/FVC < 70 % and FEV1 < 50%), heart failure(NYHA score =III、IV), kidney failure(eGFR< 60 ml.min-1.1.73m-2), liver failure
  • patients with ongoing infection
  • patient allergic to voluven

研究组 & 干预措施

Intubated group

Experimental

Patient in this group will receive general anesthesia with endotracheal tube intubation to perform one lung ventilation. Patient will be paralyzed and controlled ventilation will be implied.

干预措施: Crystalloid Solutions (Drug)

Non-intubated group

Experimental

Patient in this group will receive general anesthesia with laryngeal mask insertion. Patients in this group will not be paralyzed and keep spontaneous breathing to maintain one lung ventilation.

干预措施: Crystalloid Solutions (Drug)

结局指标

主要结局

Change of blood pressure after fluid loading

时间窗: 3 hours

Interpretate the correlation of mini-fluid challenge and conventional fluid challenge

次要结局

  • Change of cardiac index after fluid loading(3 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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