Emergency Room Analgesia and Sedation Survey-2
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 13,000
- 主要终点
- Cognitive score
研究概览
简要总结
Part 1: Assessment of Healthcare Providers' Knowledge on Analgesia and Sedation in Emergency Resuscitation Rooms Across China This study aims to evaluate the understanding of healthcare providers in emergency resuscitation rooms regarding the principles of analgesia and sedation, commonly used assessment tools, and delirium management, and to identify key factors that may influence their level of knowledge. Part 2: Implementation Practices of Analgesia and Sedation in Emergency Resuscitation Rooms Across China: A Multicenter Prospective Cohort Study Primary Objective: To assess the extent of adherence to standardized protocols for analgesia and sedation in emergency resuscitation rooms of general hospitals in China. Secondary Objectives: (1) To identify key factors affecting compliance with standardized analgesia and sedation practices in emergency resuscitation settings, thereby providing evidence for targeted interventions; (2) To examine the impact of analgesia and sedation implementation on clinical outcomes and prognosis of patients in emergency resuscitation rooms.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 120 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •: Part 1: (1) Healthcare professionals currently assigned to the emergency department and actively working in the emergency resuscitation room; (2) With at least one year of clinical experience in emergency medicine; (3) Willing to voluntarily participate in the investigation. Each participating institution is required to enroll a minimum of 12 healthcare providers, including at least 6 physicians and 6 nurses. Within each group (physicians and nurses), at least 3 participants must hold junior professional titles and at least 3 must hold intermediate or senior-level professional titles.
- •Part 2: All adult patients (≥18 years of age) admitted to the emergency resuscitation room during the period from July 15, 2025 to July 30, 2025.
排除标准
- •Pregnant women
- •patients undergoing end-of-life care
- •individuals incapable of providing informed consent
- •patients who decline participation.
结局指标
主要结局
Cognitive score
时间窗: At the time of inclusion in the study
The cognitive scores obtained through questionnaire surveys
次要结局
未报告次要终点
