NCT03438578已完成不适用
Use of Efficacy Safety Score in Postoperative Management: A Prospective, Randomized Study
St. Olavs Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年3月5日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Time to Mobilization
研究概览
简要总结
The primary aim of this project is to determine whether postoperative patients may benefit from the Efficacy Safety Score (ESS) as a tool for postoperative clinical decision support, with a special focus on the first 24 hours after discharge from the postoperative care unit.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
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
- •undergoing surgery
- •expectedly to be treated and observed in hospital for more than 24 hours postoperatively
排除标准
- •refusal of participation
- •poor communication capabilities
结局指标
主要结局
Time to Mobilization
时间窗: 24 hours
The measured postoperative time when patient can stand and able to walk one or more steps, with or without support
次要结局
- Pain Measurement, Verbal Numeric Rating Scale(24 hours)
- Patient Satisfaction(24 hours)
研究者
研究点 (1)
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