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临床试验/NCT01225692
NCT01225692已完成不适用

Brain Trauma Outcomes in Nova Scotia

Queen Elizabeth II Health Sciences Centre0 个研究点目标入组 52 人开始时间: 2004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
52
主要终点
Time Measurement; Hours:minutes

研究概览

简要总结

The goals of this study are to identify outcome indicators of optimal care for brain injury patients, including pre-hospital care, prompt delivery to neurosurgical care and access to early rehabilitation services. Nova Scotia's centralized Neurosurgical services and integrated provincial Emergency Health Services provide a rich opportunity to construct a cohesive, integrated data management system. This system will allow us to answer important research questions related to the outcomes, care and prevention of brain trauma.

Retrospective data collection The retrospective arm of the BTO study has created full data sets and care pathways from multiple sources covering the continuum of brain trauma care. Investigators continue to analyze this large amount of data and prepare it for publication.

Prospective data Collection Patients with a major head injury (initial GCS 3-12), have been considered for enrollment in the BTO study.The prospective arm of the BTO study has 52 patients enrolled. Screening and Enrollment was complete on June 30, 2007. These patients are participating in long term follow up at 6, 12 and 24 months post injury for assessment of qualitative and quantitative outcomes. Completion of patient follow up will be in June 2009.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research

入排标准

性别
All
接受健康志愿者

入选标准

  • 1.patient treated in at least one facility prior to arrival at QEII.
  • Exclusion Criteria
  • injured out of province
  • time from injury to 1st facility presentation known to be > 24 hours
  • time arrival at 1st referring facility to time arrive at QEII known to be > 24 hours
  • direct ground or air scene transport
  • Prospective Arm:
  • Inclusion Criteria:
  • have a head injury requiring hospital admission
  • able to provide informed consent or have next- of -kin able to provide consent on patients' behalf

排除标准

  • unwilling or unable to provide consent

结局指标

主要结局

Time Measurement; Hours:minutes

Time as measured by ; Time Elapsed from Injury Time to Time of Arrival at Tertiary Care

次要结局

  • Clinical Follow-up; Numerical Score 1-5;Glasgow Outcome Scores (GOS)

研究者

申办方类型
Other

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