跳至主要内容
临床试验/NCT00604773
NCT00604773已完成不适用

Incidence of Delirium in Critically Ill Patients in a Dutch University Hospital

Radboud University Medical Center1 个研究点 分布在 1 个国家目标入组 700 人开始时间: 2008年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
700
试验地点
1
主要终点
delirium

研究概览

简要总结

The objective of this study is to determine the incidence of delirium in adults patients who are admitted at the critical care unit of a Dutch University Hospital.

The primary aim is to determine the incidence of delirium and to determine risk factors for this group of patients to develop a prediction model.

A secondary aim is to find differences between delirious patients and non-delirious patients on different aspects of diagnostics, treatment and care, outcome, length of stay, and inflammation.

According to Dutch law, the need to obtain informed consent was waived by the Committee on Research Involving Human Subjects (CMO) of Nijmegen for this observational study (2007/283).

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

  • all adult patients (18 years and older) admitted at the critical care unit of our hospital

排除标准

  • not able to understand Dutch
  • patients with serious hearing and visibility disabilities
  • mentally retarded patients

结局指标

主要结局

delirium

时间窗: during admission at the critical care

次要结局

  • biomarkers(within 24 hours of delirium diagnosis)
  • markers of inflammation(within 24 hours of delirium diagnosis)

研究者

申办方类型
Other

研究点 (1)

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