PACTR201708002325400已完成未知
A randomized controlled trial comparing the proportion of hypoxia in sedated adults undergoing upper gastrointestinal endoscopy using target controlled infusion of propofol versus intermittent boluses.
The Aga Khan University, Nairobi0 个研究点目标入组 176 人开始时间: 2017年5月26日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 176
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Year(s) 至 65 Year(s)（—）
- 性别
- All
入选标准
- •All ASA I and II adults aged 18 - 65 years scheduled to undergo non-emergent upper gastrointestinal endoscopy under sedation.
排除标准
- •¿Known allergy to propofol, midazolam, soybean, egg.
- •¿Active respiratory tract infection.
- •¿History or indicator of large airway compromise e.g. obstructive sleep apnoea, COPD, presence of stridor, or known history of difficult bag-valve-mask ventilation.
- •¿Patients requiring additional types of sedative agents to achieve optimal sedation.
- •¿History of chronic exposure to sedative medication.
研究者
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