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临床试验/NL-OMON23993
NL-OMON23993已完成不适用

A randomized controlled trial of respiratory function monitoring during stabilization of preterm infants at birth

eids Universitair Medisch Centrum, Leiden, The Netherlands0 个研究点目标入组 320 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
320

研究概览

简要总结

/A

研究设计

研究类型
Observational

入排标准

入选标准

  • Infants born will be included in this study if they are between 24 and 27 completed weeks gestation receiving PPV for resuscitation at birth and do not have a known abnormality which might interfere with breathing.

排除标准

  • Infants will be excluded from the final analysis if they are found to have a congenital abnormality or condition that might have an adverse effect on breathing or ventilation, including: congenital diaphragmatic hernia, tracheo-oesophageal fistula or cyanotic heart disease.

研究者

发起方
eids Universitair Medisch Centrum, Leiden, The Netherlands

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