跳至主要内容
临床试验/NCT03438578
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

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

发起方
St. Olavs Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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