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临床试验/NCT03226964
NCT03226964已完成不适用

Assessment of High Flow Nasal Cannula Oxygenation in EBUS Bronchoscopy

University College Hospital Galway1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
drop in oxygen saturation during procedure

研究概览

简要总结

This study is a prospective randomised trial where a computer will randomly allocate

patients to one of two possible methods of delivering oxygen during the procedure of

bronchoscopy. This trial compares high flow nasal cannula (HFNC) with nasal prongs in

delivering oxygen to patients undergoing endo-bronchial ultrasound guided trans-

bronchial nodal aspiration (EBUS-TBNA) a specialised form of bronchoscopy procedure.

HFNC uses humidified higher gas flow rates than conventional low flow systems such as

nasal prongs which are limited by the respiratory rate and effort.

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

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with a peripheral arterial pulse oximetry ≥ 90% breathing room air
  • Age ≥ 18 years
  • Able to breathe spontaneously throughout the procedure

排除标准

  • Respiratory or cardiac failure
  • Recent myocardial infarction < 6 weeks ago
  • On long term oxygen therapy, those with tracheostomy and/ or non-invasive or invasive mechanical ventilation
  • Nasal and/ or nasopharyngeal disease
  • Inability to give informed consent
  • Hepatic or end stage renal disease
  • Pregnancy

结局指标

主要结局

drop in oxygen saturation during procedure

时间窗: through procedure completion defined as withdrawing scope from patient's mouth, an average of 30 minutes

the difference in oxygen saturation levels between pre-treatment assessments and the lowest saturation level achieved during treatment

次要结局

  • change in venous CO2(1 hour after procedure)
  • end tidal CO2 during procedure(through procedure completion defined as withdrawing scope from patient's mouth an average of 30 minutes)
  • Patient experience measure on a visual analogue scale(up to 3 hours after procedure)
  • endotracheal intubation during or post procedure(24 hours)

研究者

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

Mohammed Ahmed

Specialist Registrar in Respiratory Medicine

University College Hospital Galway

研究点 (1)

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