跳至主要内容
临床试验/NL-OMON26151
NL-OMON26151招募中不适用

Postoperative cognitive dysfunction in elderly cancer patients

niversity of Groningen0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
150

研究概览

简要总结

one.

研究设计

研究类型
Observational

入排标准

入选标准

  • Surgery is scheduled more than 24 hours after inclusion in the study as we feel this is the time necessary to obtain test results and plan the intraoperative recording of data.
  • - surgery under general, local or regional anesthesia.
  • - written informed consent given according to local regulations.

排除标准

  • - any physical condition potentially hampering complicance with the study protocol and follo up schedule, this includes: severe visual impairment, total deafness or the inability to hold a pencil.
  • - personal time constraints unabling patients to comply to the study protocol.
  • - patients unable to comply with the outcome questionnaires (this includes insufficient knowledge of the Dutch language).

研究者

发起方
niversity of Groningen

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