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临床试验/NCT01786642
NCT01786642Unknown不适用

Assessment of the Efficacy of Tracheal Oxygen Administration During Bronchoscopy - a Phase II Trial.

KU Leuven1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2013年2月最近更新:
适应症

试验速览

阶段
不适用
发起方
KU Leuven
入组人数
40
试验地点
1
主要终点
Time to correction of SpO2

研究概览

简要总结

The aim of the present study is to measure the time to correction of O2 saturation when in case of desaturation below 90%, O2 administration is switched from the nasal to the tracheal route at a similar flow rate.

详细描述

The development of a flexible bronchoscope with a channel dedicated to O2 administration might allow optimization of the oxygen supplementation during bronchoscopy, which reduces the risk of per- and peri-procedural hypoxemia. The investigators will conduct a pilot study corroborating the hypothesis that tracheal supplementation of oxygen during flexible bronchoscopy is advantageous in comparison to nasal cannula supplementation.

The concept of our trial consists of a mono-centric observational study performed in the endoscopy suite of the Respiratory Division, University Hospitals Leuven. All patients will be given informed consent before inclusion.

The aim of the present study is to measure the time to correction of O2 saturation when in case of desaturation below 90%, O2 administration is switched from the nasal to the tracheal route at a similar flow rate.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • patients referred for flexible bronchoscopy

排除标准

  • broncho-alveolar lavage
  • endobronchial plugging

结局指标

主要结局

Time to correction of SpO2

时间窗: procedure

次要结局

未报告次要终点

研究者

发起方
KU Leuven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marc Decramer

MD, PhD

KU Leuven

研究点 (1)

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