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临床试验/NCT04261231
NCT04261231已完成不适用

Correlation of the "Preliminary Universal Surgical Invasiveness Score" (pUSIS) With Short Term Post-operative Clinical Outcome Parameters. An Observational Study

University of Zurich1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
Duration of postoperative hospital stay

研究概览

简要总结

The scope of this investigation is to demonstrate that the pUSIS values correlate closely with short term post-operative clinical outcome parameters, thus making this scoring system a good predictor for the patients' postoperative course and may become a helpful instrument for decision making concerning the choice of postoperative surveillance and treatment. The obtained follow up results were subjected to correlation analyzis with the pUSIS values in order to determine their association and if possible to recognize threshold values that may indicate a suitable type/intensity of postoperative surveillance.

详细描述

a number of 60 day-care as well as 100 in-hospital patients undergoing elective surgery in general anesthesia have been enrolled into this observational study. The recruitment of cases happened randomly on a daily basis according to the available operations in the surgical unit where the main investigator (NN) was performing her/his anesthesiological services. Thus there was no selection of specific surgeries or surgical disciplines.

Inclusion criteria: adult patients (>18 y) undergoing surgery in general anesthesia.

Exclusion criteria: emergency cases, patients aged < 18 years, pregnant women, inability to give informed consent.

The data acquisition consisted of calculation of the individual pUSIS for the selected cases by end of surgery, and by collecting in the follow up period the following set of short term parameters:

In-hospital patients

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • adult patients (>18 y) undergoing surgery in general anesthesia

排除标准

  • emergency cases
  • patients aged < 18 years
  • pregnant women
  • inability to give informed consent

结局指标

主要结局

Duration of postoperative hospital stay

时间窗: 1-60 days

In-hospital days

Duration if intensive care treatment

时间窗: 600 hours

ICU hours

Duration of postoperative ventilation

时间窗: 600 hours

Ventilation hours

Postoperative complications

时间窗: 1-60 days

thromboembolic, hepato-renal, neorologal, infections

次要结局

  • Subjective wellbeeing(1-60 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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