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临床试验/NCT03291184
NCT03291184已完成不适用

Is Postoperative Residual Curarisation Still an Issue at the Moment of Weaning of the ICU Patient Following Cardiac Surgery?

Onze Lieve Vrouw Hospital2 个研究点 分布在 1 个国家目标入组 93 人开始时间: 2017年9月4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
93
试验地点
2
主要终点
postoperative residual curarisation

研究概览

简要总结

The main objective of this study is to describe the incidence of postoperative residual paralysis (mean train-of-four <90%) when weaning from the ventilator in patients admitted to the Intensive Care Unit (ICU) after elective cardiac surgery. Train-of-four monitoring is a widely used term for the peripheral nerve stimulation used in neuromuscular blockade monitoring. When the patient is ready for weaning from the ventilator, an ICU doctor will perform a measurement of the train-of-four at the thumb with a neuromuscular transmission monitor. Every value below 90% will be considered as residual paralysis and treated appropriately by means of a reversal agent.

详细描述

Postoperatively, in the ICU, readiness-for-weaning is based on ICU doctor-nurse-driven institutional weaning guidelines: 6 hours after arrival in the ICU, a patient who is normothermic, hemodynamically stable, has normal blood gasses and absence of residual bleeding. The ICU nurse caring for the patient will start weaning the patient from the ventilator, following these departmental guidelines.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
Double (Participant, Investigator)

盲法说明

The participant will still be under sedation at the moment of measuring neuromuscular blockade. The care provider will perform measurements, while the investigator is blinded.

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients admitted to the ICU after elective cardiac surgery

排除标准

  • emergency cardiac surgery

结局指标

主要结局

postoperative residual curarisation

时间窗: 6 hours after arrival in the ICU

mean train-of-four \<90% as measured by neuromuscular blockade monitoring

次要结局

未报告次要终点

研究者

发起方
Onze Lieve Vrouw Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Guy CAMMU

MD, PhD, Staff Anesthesiologist

Onze Lieve Vrouw Hospital

研究点 (2)

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