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临床试验/ACTRN12623000575639
ACTRN12623000575639尚未招募Unknown

aryngeal oxygen concentration and apnoea time during microlaryngeal surgery using transnasal humidified rapid-insufflation ventilatory exchange (THRIVE) with different oxygen concentrations: A randomised controlled clinical trial

Dr Liang Voice Program, The University of Sydney0 个研究点目标入组 102 人开始时间: 2023年5月25日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
102

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Age > 18 years
  • - Elective microlaryngeal surgeries, including but not limited to the following procedures:
  • Microlaryngoscopy with or without biopsy (MBS item number: 41855)
  • Microlaryngoscopy with removal of laryngeal lesion (MBS item number: 41861)
  • Microlaryngoscopy with removal of lesion including laser (MBS item number: 41861)
  • Microlaryngoscopy and laryngeal injection (MBS item number: 41870)
  • Microlaryngoscopy and treatment of subglottic stenosis
  • - Willingness of the participant’s treating anaesthetist to enrolthe participant, in the absence of any identified contraindications.

排除标准

  • - Baseline oxygen saturation level less than 95%
  • - Know history of lung disease, including but not limited to COPD and Type I or Type II respiratory failure.
  • - Body Mass Index (BMI) greater than 31.

研究者

发起方
Dr Liang Voice Program, The University of Sydney

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