跳至主要内容
临床试验/NCT02143128
NCT02143128已完成不适用

Safety and Quality for Inpatients After Surgery at the Ward. Development and Evaluation of a New Tool: Efficacy Side-effect Score (ESS)

Vestre VikenHF Kongsberg Sykehus3 个研究点 分布在 2 个国家目标入组 1,152 人开始时间: 2014年3月1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
1,152
试验地点
3
主要终点
Length of Hospital Stay (LOS)

研究概览

简要总结

We hypothesized that better control of postoperative pain treatment and its side effects by monitoring ESS might influence the degree of mobility and morbidity in surgical patients and consequently reduce LOS. Thus, our aim was to validate the influence of recording ESS and the application of a "call-out algorithm" on LOS in two university hospitals in which the routine policy of registration of pain had not been adopted yet.

详细描述

Using clinical experience and consensus-methodology the investigators picked up and digitalized information about mental, postoperative nausea, vomiting and pain status at the rest and during mobilization in so called Efficacy Safety Score (ESS). Depending on expression of patient's complaints, all mentioned above clinical features are scored. We hypothesized that better control of postoperative pain treatment and its side effects by monitoring ESS might influence the degree of mobility and morbidity in surgical patients and consequently reduce length of hospital stay (LOS). Thus, our aim was to validate the influence of recording ESS and the application of a "call-out algorithm" on LOS in two university hospitals in which the routine policy of registration of pain had not been adopted yet. The primary endpoint of the study was to assess LOS in groups of patients with different types of clinical data records and "call-out algorithms," while secondary endpoints were to compare the degree of mobilization, number of postoperative nonsurgical complications, and 28-day survival between the groups.and summarized in the total score.

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

  • All adult postoperative patients that are inpatients, and scheduled for hospitalization for more than 8 hours

排除标准

  • Children, mental illness, communication difficulties

结局指标

主要结局

Length of Hospital Stay (LOS)

时间窗: 28 days

Assess LOS in groups of patients with different types of clinical data records an "all-out algorithms"

次要结局

未报告次要终点

研究者

发起方
Vestre VikenHF Kongsberg Sykehus
申办方类型
Other
责任方
Principal Investigator
主要研究者

Erlend Johan Skraastad

Consultant, MD

Vestre VikenHF Kongsberg Sykehus

研究点 (3)

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