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临床试验/NCT04439968
NCT04439968进行中(未招募)不适用

Targeted Cerebral Saturations in Extremely Preterm Infants

Stanford University2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年8月10日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
100
试验地点
2
主要终点
Neurodevelopmental outcome

研究概览

简要总结

Implementing target ranges for regional cerebral saturations in extremely preterm infants in the first week of life may improve neurodevelopmental outcomes at 22-26 months corrected age compared to those without targeted cerebral saturations (Csat) using near-infrared spectroscopy (NIRS). Infants will be randomized to a targeted cerebral saturation monitoring group with visible reading of Csat or to a control group with cerebral saturation monitoring, but with blinded Csat measures. Those in the targeted Csat group will follow a treatment guideline to maintain cerebral oxygenation in the target range. The primary outcome is neurodevelopmental outcome as determined by Bayley III cognitive scale score.

研究设计

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

盲法说明

Assessors of neurodevelopmental outcome are blinded to targeted vs non-targeted monitoring

入排标准

年龄范围
— 至 2 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Very preterm infants with gestational age at least 23 weeks but less than 29 completed weeks
  • Less than 6 hours of age

排除标准

  • Skin integrity insufficient to allow placement of NIRS sensors
  • Decision not to provide full intensive care support
  • Congenital condition, other than premature birth, that adversely affects life expectancy or neurodevelopment

结局指标

主要结局

Neurodevelopmental outcome

时间窗: 22-26 months of age

Neurodevelopmental outcomes will be assessed using the cognitive component of the Bayley Scales of Infant Development-III at 22-26 months of age. Scores range from 55-145 with higher number representing a better neurodevelopmental outcome.

次要结局

  • Death(from birth until hospital discharge, an average of 3 months.)
  • Retinopathy of prematurity(from birth until hospital discharge, an average of 3 months.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Valerie Chock, M.D., M.S. Epi

Principal Investigator

Stanford University

研究点 (2)

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