NCT06012955招募中不适用
Study on the Effect of Target-controlled Infusion of Propofol and Remifentanil for Patients Undergoing Cardiac Surgery
Wuhan Union Hospital, China1 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2023年8月30日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 2,000
- 试验地点
- 1
- 主要终点
- Duration of postoperative mechanical ventilation
研究概览
简要总结
The purpose of the study was to evaluate whether individualized general anesthesia with target-controlled infusion could help patients wake up early for extubation and reduce the incidence of postoperative complications, and to investigate the effectiveness and safety of its application in patients undergoing cardiac surgery.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
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
- •All patients aged 18 years and older who underwent cardiac surgery
排除标准
- •Mechanical ventilation support before surgery;
- •Combined with any type of non-cardiac surgeries;
- •Second exploratory thoracotomy after surgery;
- •Died or discharged within 48 h after surgery;
- •Missing clinical data
结局指标
主要结局
Duration of postoperative mechanical ventilation
时间窗: 4 weeks after surgery
Duration of mechanical ventilation was defined as the time from the end of surgery to tracheal extubation
次要结局
未报告次要终点
研究者
研究点 (1)
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