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临床试验/NCT04438798
NCT04438798Unknown不适用

A Prospective Randomized Study of High Flow Nasal Cannula to Prevent Deoxygenation During Induction of General Anesthesia in Cesarean Section

Alexandria University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2020年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
80
试验地点
1
主要终点
measure the time of safe apnea

研究概览

简要总结

Transnasal humidified rapid-insufflation ventilatory exchange (THRIVE) using high flow oxygen therapy for preoxygenation and oxygen supplementation during apnoea has shown promising results

详细描述

Eeffective preoxygenation followed by apnoeic oxygenation enables anaesthesiologists to safely prolong the apnoea time which is the time (seconds) of apnea following preoxygenation and muscle relaxation before to peripheral oxygen saturations (SpO2) decreases by 2%.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Participant)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •pregnant females
  • •Of American Society of Anesthesiologists (ASA) physical Status I and II
  • •For elective cesarean section under general anesthesia

排除标准

  • •with room air saturation of <98%
  • •anticipated difficult airway
  • •anticipated obstetric risk factor or precious baby
  • •chronic obstructive pulmonary disease
  • •thyrotoxicosis
  • •pheochromocytoma
  • •hyperkalaemia
  • •significant cardiac illness

研究组 & 干预措施

face mask group

Placebo Comparator

Pregnant females will be preoxygenated with 100% oxygen using a tight-fitting face mask at a rate of 6 L/min for 3 min with end-tidal gas monitoring.

干预措施: F Group (Other)

THRIVE group

Active Comparator

High-flow humidified oxygen warmed to 37°C will be delivered through nasal cannula at the rate of 30 L/ min for 30 seconds then 50 liters per minute for a further 150 seconds.

干预措施: H Group (Other)

结局指标

主要结局

measure the time of safe apnea

时间窗: 10 minutes after induction

The apnea time will start from the onset of cessation of breathing as evidenced by a flat line in the capnogram with the absence of chest movements

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

rehab zayed

Assisstant Professor of Anesthesia

Alexandria University

研究点 (1)

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