跳至主要内容
临床试验/NCT05847010
NCT05847010招募中不适用

Accompanying Scientific Program for the Quality Contract Prevention of Postoperative Delirium in the Care of Older Patients (WB-QC-POD)

Charite University, Berlin, Germany1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年6月22日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
1
主要终点
Incidence of postoperative Delirium

研究概览

简要总结

In the course of a scientific accompanying program, the project pursues the goal of gaining further insight into a possible connection between various influencing factors and the development of postoperative delirium. Against this background, in addition to the primary goal of exploring delirium rates, we aim to identify associations between other secondary end goals like the internal circadian time or the heart rate variability and the occurrence of postoperative delirium. For this purpose, patients of the QC-POD (NCT04355195) sample will be studied.

详细描述

The project aims to improve the understanding of the internal circadian time (chronotype) and other sleep parameters, as well as further secondary end goals, in relation to the development of postoperative delirium. In the course of this the project would like to investigate the perioperative heart rate variability. Also, the association of perioperative peripheral cholinesterase activity with perioperative heart rate variability and the development of POD will be explored. Additionally, the investigator will analyze the correlation of intraoperative EEG signatures with perioperative heart rate variability, and explore any association of core body temperature and the development of postoperative Delirium.

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
70 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 70 years
  • Male and female patients
  • Patients who have been included in QC-POD
  • Eligible patients* for inclusion: informed consent by the patient, preoperatively with verbal and written informed consent before the start of data collection
  • Incapacitated patients for inclusion: Written informed consent by a legal representative
  • surgery (elective and not elective)

排除标准

  • Moribund patients (palliative situation)
  • Insufficient knowledge of the German language
  • Cardiac arrhythmia (e.g. atrial fibrillation)
  • Presence of a pacemaker
  • Condition after heart transplantation
  • Inflammation in the area of the frontal sinus

结局指标

主要结局

Incidence of postoperative Delirium

时间窗: Up to the fifth postoperative day

Incidence of postoperative delirium in all postoperative patients in normal ward, intensive care unit and recovery room with a validated delirium screening tool at two points in time.

次要结局

  • Duration of Delirium(The participants are followed up until the end of hospital stay, an expected average of 7 days)
  • Bodytime(Before surgery)
  • Chronotype 1(Up to three months)
  • Chronotype 2(Up to three months)
  • Heart rate variability 1(The participants are followed up until the end of hospital stay, an expected average of 7 days.)
  • Heart rate variability 2(The participants are followed up until the end of hospital stay, an expected average of 7 days.)
  • Body core temperature(Up to the third postoperative day)
  • Electroencephalography signatures(During surgery, an expected time of two hours.)
  • Sleep monitoring 1(Up to the third postoperative day)
  • Sleep monitoring 2(Up to the third postoperative day)
  • Sleep monitoring 3(Up to the third postoperative day)
  • Insomnia Severity Index(Up to three months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Claudia Spies

Head of the Department of Anesthesiolgy and Intensive Care Medicine CC07

Charite University, Berlin, Germany

研究点 (1)

Loading locations...

相似试验

Accompanying Scientific Program for the Quality... | 临床试验