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临床试验/NL-OMON55817
NL-OMON55817招募中不适用

Prediction and recovery of cognitive impairment in neurosurgical patients. - Predict

Elisabeth-Tweesteden ziekenhuis0 个研究点目标入组 1,230 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
1,230

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • The study sample will be composed of patients admitted for intracranial
  • neurosurgical treatment of brain tumours (e.g., meningiomas, adenomas, gliomas
  • or metastases), vascular compression syndromes (e.g., trigeminal neuralgia) or
  • lesions (e.g., aneurysms)., Eligible subjects for the control group are:
  • 1) sociodemographically similar to the patient group
  • 2) in good health, with no current or past psychiatric, neurologic, or
  • cognitive disorder, and mediation-use that interferes with cognitive function

排除标准

  • Patients and Dutch control subjects will be excluded from participation in this
  • 1) if lack basic proficiency in Dutch
  • 2) if their IQ is below 85 or if they have low cognitive skills
  • 3) if their Karnovsky Performance Scale is under 60
  • 4) if they are completely unfamiliar with the use of computers
  • 5) if they have an additional (history of) a significant neurological or
  • psychiatric disorder
  • 6) if there is no surgery-related complication (morbidity or mortality due to
  • e.g., thrombosis or heart attack)
  • [APOE substudy: objection against 'further use' of samples of previously drawn

研究者

发起方
Elisabeth-Tweesteden ziekenhuis

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