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临床试验/NL-OMON50369
NL-OMON50369招募中不适用

Comparative effectiveness research within the Dutch Neurotraumatology Quality Registry. - Net-QuRe

eids Universitair Medisch Centrum0 个研究点目标入组 1,000 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
入组人数
1,000

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
12 至 99(—)

入选标准

  • Presentation within 24 hours of injury.
  • Clinical diagnoses traumatic brain injury.
  • GCS < 13 by presentation ER.
  • Secundair decrease (GCS < 13) <= 24 hours after presentation on the ER.
  • Informed Consent obtained according to local and national requirements.
  • Age 16 year or older.

排除标准

  • Severe pre-existing neurological disorder that would confound outcome
  • assessments.
  • By presentation a not traumatic cause of decreased consciousness.
  • Insufficient knowledge of Dutch or English language.

研究者

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