NCT01979549Unknown不适用
Adverse Events During Upper Gastrointestinal Endoscopy With and Without Sedation: a Multiple Center Report From Shanghai
适应症
试验速览
- 阶段
- 不适用
- 入组人数
- 6,000
- 试验地点
- 3
- 主要终点
- Adverse events
研究概览
简要总结
The primary objective is to investigate the adverse events during upper gastrointestinal endoscopy with and without sedation in Chinese population
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients will undergo upper gastrointestinal endoscopy
- •Age > 18 years old
- •Signed informed consent form
排除标准
- •Allergy to propofol or soybean or albumen
结局指标
主要结局
Adverse events
时间窗: Patients will be followed for the duration of hospital stay, an expected average of 2 hours
Investigate the adverse events according to the Adverse event reporting tool of the world SIVA International Sedation Task Force during upper gastrointestinal endoscopy with and without sedation.
次要结局
未报告次要终点
研究者
研究点 (3)
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