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临床试验/NCT03705728
NCT03705728Unknown不适用

Impact of the Automated Administration of Intravenous Anesthesia Compared to Inhalatory Anesthesia on the Speed of Emergence and the Occurrence of Postoperative Delirium

Centre Clinical, France1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2018年5月30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
发起方
入组人数
1,000
试验地点
1
主要终点
Comparison of the Nurse Delirium Screening Scale in the early postoperative period between intravenous vs halogenated general anesthesia

研究概览

简要总结

The intravenous administration of anesthetic agents by a controller automatically-guided by an index of cerebral activity (i.e. the bispectral index) decreases the incidence of postoperative delirium, compared with an inhalational anesthesia.

详细描述

Scientific background Postoperative delirium (POD) is a common complication occurring in 5 to 50 % of elderly patients following an operation. Delirium is a serious complication leading to many medical as well as social and economical consequences. Several studies suggest that, both, the choice of anesthetic agents and the conduction of anesthesia might decrease the incidence of POD.

Objectives Study goal and primary aim: the intravenous administration of anesthetic agents by a controller automatically-guided by an index of cerebral activity (i.e. the bispectral index) decreases the incidence of POD, compared with an inhalational anesthesia.

The primary aim of the present study (i.e. incidence of POD) will be assessed by the Nursing Delirium Screening Scale (NDSS).

Secondary aims:

Secondary aim 1: Assessment of a potential difference on the incidence of PONV between the 2 groups of patients (i.e. intravenous vs. inhaled) by comparison of the number of episodes of nausea and vomiting and the need to treat this complications, between both groups.

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
Double (Participant, Care Provider)

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 > 59 year
  • Informed written consent before enrolment;
  • Procedure duration > 60 min.
  • Speaking French
  • Possible contact one-month following surgery

排除标准

  • Contraindication of brain monitoring (intracranial surgery), pace-maker.
  • Propofol or remifentanil allergy.
  • Patients under guardianship

研究组 & 干预措施

Intravenous group

Experimental

Propofol & remifentanil administration using the closed-loop controller with the "Easy-TIVA" platfrom.

干预措施: Propofol (Drug)

Intravenous group

Experimental

Propofol & remifentanil administration using the closed-loop controller with the "Easy-TIVA" platfrom.

干预措施: Remifentanil automatic (Drug)

volatile anesthesia group

Active Comparator

Sevoflurane will be administered manually according to the BIS values. Remifentanil will be administered manually using a Target Controlled Infusion pump using the Minto model.

干预措施: Sevoflurane (Drug)

volatile anesthesia group

Active Comparator

Sevoflurane will be administered manually according to the BIS values. Remifentanil will be administered manually using a Target Controlled Infusion pump using the Minto model.

干预措施: Remifentanil manual (Drug)

结局指标

主要结局

Comparison of the Nurse Delirium Screening Scale in the early postoperative period between intravenous vs halogenated general anesthesia

时间窗: Measure of the Nurse Delirium Screening Scale, up to an estimated maximum of 3 hours postoperatively

occurrence of POD as measured by the Nursing Delirium Screening Scale The Nursing Delirium Scale Symptom Symptom rating Disorientation 0 points 1 point 2 points Inappropriate behavior 0 points 1 point 2 points Inappropriate communication 0 points 1 point 2 points Illusion/hallucination 0 points 1 point 2 points Psychomotot retardation 0 points 1 point 2 points Total score ≤ 2 points \> 2 points Delirium No Yes

次要结局

未报告次要终点

研究者

发起方
Centre Clinical, France
申办方类型
Other
责任方
Sponsor

研究点 (1)

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