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临床试验/NCT02501681
NCT02501681已完成4 期

Evaluation of Different Priming Solutions Effects on Microcirculation, Oxidative Stress and Morbidity in Cardiovascular Surgery Patients

Medical Centre Leeuwarden1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2015年2月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
change in microvascular flow index (MFI)

研究概览

简要总结

Single-centre prospective randomized study will be included the patients who undergo elective cardiovascular surgery. Preoperative fluid deficit will be calculated by the formula as starvation period X 4 X weight. Patients will be divided into two groups: Group A (n=20); crystalloid as priming solution used in patients, Group B (n=20); colloids as priming solution used in patients. In addition to priming solutions, extracorporeal pump will be filled with 150 mL of Mannitol, 60 mL of NaHCO3 and 10000 IU Insulin. Standard anesthesia protocol will be administered to all patients. Ringer's Lactate will be given at first 30 minute after induction. Ringer's Lactate as fluid maintenance will be administered at a rate of 100 mL/h except in extracorporeal circulation. Goal-directed fluid management will be performed by PVI (Pleth Variability Index). Cut off level of PVI will be accepted %15.

详细描述

For integrative investigation of the effects of priming solution and postoperative fluid management on the complex interrelation between microcirculation and reactive oxygen species; sublingual microcirculation using microcirculation imaging system (IDF, Cytocam, NL) will be displayed and measure ekstra vascular lung water (EVLW) using PiCCO and plasma levels of oxidative stress markers will be measured. Sublingual tissue microcirculation will be evaluated in all patients at different time points as before induction (T0), after induction (T1), before cross clamping-hypothermic period (T2), after cross clamping (T3), before end of pump (normothermic period, heating) (T4), acceptance to intensive care unit (T5), third hour after surgery (T6) and twenty forth hour after surgery (T7).

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
否

入选标准

  • •cardiovascular surgery needed

排除标准

  • •no informed consent

研究组 & 干预措施

crystalloid

Active Comparator

Group A (n=20); crystalloid as priming solution used in patients,

干预措施: priming solution during cardiovascular surgery (Other)

colloid

Active Comparator

Group B (n=20); colloids as priming solution used in patients

干预措施: priming solution during cardiovascular surgery (Other)

结局指标

主要结局

change in microvascular flow index (MFI)

时间窗: 1 day

hemodilution by the priming solutions in extracorporeal circulation affects the sublingual microcirculation

次要结局

  • difference in MFI(1 day)

研究者

发起方
Medical Centre Leeuwarden
申办方类型
Other
责任方
Principal Investigator
主要研究者

Matty Koopmans

MSc

Medical Centre Leeuwarden

研究点 (1)

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