A Randomized Controlled Trial Comparing Nasal With Buccal Oxygen Administration for Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- hypoxia-related interruptions
研究概览
简要总结
The purpose of this study is to compare to nasal and buccal oxygen administration in patients undergoing Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration .
详细描述
Anesthesia for Endobronchial Ultrasound (EBUS) may be range from routine bronchoscopy sedation to general anesthesia. During sedation to EBUS increased duration of anesthesia and sedative dosing put patients at increased risk for hypoxic events. To avoid this, oxygen supplementation is mandatory. There are different techniques for oxygen supplementation during the procedure. At this study we will compare to nasal and buccal oxygen supplementations during EBUS.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 90 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •patients ≥18 years of age
- •body mass index (BMI) between 20 and 30
- •American Society of Anesthesiologists physical status I-III
排除标准
- •congestive heart failure
- •ischemic heart disease
- •increased intracranial pressure
- •known allergy or contraindication to study drugs (propofol, fentanyl, or midazolam)
- •an anatomical feature precluding adequate positioning of the buccal device.
结局指标
主要结局
hypoxia-related interruptions
时间窗: 30 minutes
the number of hypoxia-related interruptions
次要结局
- duration of procedure(30 minutes)
- satisfaction of pulmonary specialist(30 minutes)
- use of propofol(30 minutes)
- use of fentanyl(30 minutes)
