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临床试验/NCT00222742
NCT00222742终止3 期

Pediatric Traumatic Brain Injury Consortium: Hypothermia

Phoenix Children's Hospital59 个研究点 分布在 6 个国家目标入组 90 人开始时间: 2007年11月最近更新:
适应症

试验速览

阶段
3 期
状态
终止
入组人数
90
试验地点
59
主要终点
The primary specific aim of this RCT is to determine the effect of induced moderate HYPO (32-33 °C) after severe TBI in children on mortality.

研究概览

简要总结

The primary hypothesis for this application for a multicenter phase III randomized clinical trial (RCT) is that induced moderate hypothermia (HYPO) (32-33 °C) after severe traumatic brain injury (TBI) in children and maintained for 48 hours will improve mortality at 3 months and 12 month functional outcome as assessed by the Glasgow Outcome Scale (GOS).

详细描述

The primary specific aim of this RCT is to determine the effect of induced moderate HYPO (32-33 °C) after severe TBI in children on mortality at 3 months post injury. The primary outcome measure will be the GOS; the primary time point for evaluation is 3 months. Further secondary functional outcome measures will include the GOS - Extended Pediatrics (GOS - E Peds), and Vineland Adaptive Behavior Scale (VABS) and will be assessed in conjunction with the GOS at 6 and 12 months post injury.

The secondary hypotheses are based on the results and analysis of the Pilot Clinical Trial (completed and recently published [Adelson et al. NEUROSURGERY. 56 (4): 740-754, 2005]). These secondary hypotheses include that induced moderate hypothermia (HYPO) (32-33 °C) after severe TBI in children and maintained for 48 h:

  • will improve other outcome assessments including neurocognitive status on performance-based neuropsychological testing across the domains of intellectual development, learning and memory, language, motor and psychomotor skills, visuo-spatial abilities, attention and executive function, and behavior at only 6 and 12 months after injury;
  • HYPO will improve long term outcome of all age ranges and across genders in infants, young, preadolescent, and adolescent children; AND
  • HYPO will lessen intracranial hypertension and lessen the intensity of therapy necessary for control of ICP.

Based on these hypotheses, further secondary specific aims are proposed:

  • Specific Aim 2: To determine the effect of early induced moderate HYPO (32-33°C) after severe TBI in children on global function and neurocognitive outcomes in the areas of intellectual ability/ development, memory and learning, and behavior at 6 and 12 months post injury.
  • Specific Aim 3: To determine the effect of early induced moderate HYPO after severe TBI in children of different age ranges (< 6 y and 6- < 16 y) on mortality and 6 and 12 months functional and neurocognitive outcomes.
  • Specific Aim 4: To determine the effect of early moderate HYPO after severe TBI in children on reducing intracranial hypertension and maintaining adequate cerebral perfusion pressure (CPP).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
— 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patients with a GCS </= 8
  • Glasgow Motor Score < 6
  • Closed head injury
  • Age 0 < 18 y
  • Exclusion Criteria
  • Unavailable to initiate cooling within 6 hours of injury
  • Glasgow Coma Scale (GCS) score = 3 and abnormal brainstem function
  • Normal initial CT scan (No blood, fracture, swelling, and/or shift)
  • Penetrating brain injury
  • No known mechanism of injury
  • Unknown time of injury
  • Uncorrectable coagulopathy (PT/PTT > 16/40 sec, INR > 1.7)
  • Hypotensive episode (Systolic Blood Pressure <5th percentile for age>10 min)
  • Documented Hypoxic episode (O2 saturation < 94% for > 30 min)

排除标准

  • 未提供

结局指标

主要结局

The primary specific aim of this RCT is to determine the effect of induced moderate HYPO (32-33 °C) after severe TBI in children on mortality.

时间窗: 3 month post injury

次要结局

  • To determine the effect of HYPO after severe TBI in children on global function and neurocognitive outcomes in the areas of intellectual ability/development, memory and learning, and behavior.(at 6 and 12 months post injury)
  • To determine the effect of HYPO after severe TBI in children of different age ranges (< 6y; 6-<16y; and 16-<18y) on mortality and 6 and 12 months functional and neurocognitive outcomes.(3, 6 and 12 months post injury)
  • To determine the effect of HYPO after severe TBI in children on reducing intracranial hypertension and maintaining adequate cerebral perfusion pressure (CPP).(7 days post injury)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (59)

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