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临床试验/NCT03903003
NCT03903003已完成不适用

In the Study; Preoperative Highflow Nasal Oxygen Application in Cesarean Under General Anesthesia and Its Effects on Newborn.

Kocaeli Derince Education and Research Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年1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
100
试验地点
1
主要终点
durations of stay

研究概览

简要总结

Preoperative Highflow Nasal Oxygen Application in Cesarean Under General Anesthesia and Its Effects on Newborn.

详细描述

Patients who will undergo caesarean section under general anesthesia will be included in the study.

In the study; preoxygenation is applied to the caesarean sections under general anesthesia in two ways. Group1 includes preoxygenation masked patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Screening
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •over 18 years old;
  • •Patients undergoing elective ceserian operation

排除标准

  • •Patients who refuse to participate in the study;
  • •Patients under emergency conditions.

研究组 & 干预措施

preoxygenation mask applied to the cesarean

Active Comparator

In order to protect the mother from hypoxia, preoxygenation is performed with face mask before induction of anesthesia.

干预措施: Face mask (Device)

high flow nasal oxygenation applied to the ceserian

Active Comparator

In order to protect the mother from hypoxia, preoxygenation is performed with high flow nasal oxygenation mask before induction of anesthesia.

干预措施: high flow nasal oxygen device (POİNT) (Device)

结局指标

主要结局

durations of stay

时间窗: 24 hours

compare the durations of stay in the intensive care unit and in hospital

次要结局

未报告次要终点

研究者

发起方
Kocaeli Derince Education and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

EMİNE YURT

clinical researcher

Kocaeli Derince Education and Research Hospital

研究点 (1)

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