跳至主要内容
临床试验/NCT05819645
NCT05819645已完成不适用

Early Versus Delayed Oral Fluid Intake Initiation (Sipping) After Extubation, Influence on the Feeling of Thirst, Patient Comfort and the Occurrence of Complications.

University Hospital, Motol1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2023年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
160
试验地点
1
主要终点
Assessment of presence or absence of thirst 120 minutes after extubation

研究概览

简要总结

According to the current guidelines the patient is not allowed to drink any fluid at least 2 hours after extubation to prevent complications. However there is no evidence in the literature to support this approach. Because anaesthetic drugs and their side effects changed significantly from their first usage, the investigators can assume that existing approach is obsolete and has no place anymore in the modern medicine. Keeping patient n.p.o (nothing per os) for 2 hours after extubation may lead to patient´s thirst or other discomfort. The aim of the study is to detect whether early oral fluid intake after extubation could lead to safe relief of thirst and to better patient´s comfort overall.

详细描述

Everything stated in the brief summary.

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

性别
All
接受健康志愿者
否

入选标准

  • •patients with planned extubation assigned to the study
  • •able to swallow the fluid
  • •willing to participate the study

排除标准

  • •patients after upper digestive tract surgery
  • •patients after trachea surgery
  • •patients with possible neurological deficiency
  • •patients after VIII. cranial nerve surgery
  • •patients not able to swallow

研究组 & 干预措施

Early fluid intake

Experimental

干预措施: Fluid intake not as per standard guidlines (Behavioral)

Standard Delayed oral fluid

Other

干预措施: Fluid intake not as per standard guidlines (Behavioral)

结局指标

主要结局

Assessment of presence or absence of thirst 120 minutes after extubation

时间窗: During procedure (120 minutes after extubation)

Between both groups the presence of anpleasent feeling of thirst will be assessed and compared

次要结局

未报告次要终点

研究者

发起方
University Hospital, Motol
申办方类型
Other
责任方
Principal Investigator
主要研究者

Durila Miroslav MUDr. Ph.D.

prf.

University Hospital, Motol

研究点 (1)

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