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临床试验/ACTRN12620000337976
ACTRN12620000337976尚未招募未知

Electrical Impedance Tomography, Thoracic Breath Sensor and Lung Ultrasound measurements of Neonates with Respiratory Distress Syndrome during surfactant administration

Mater Health0 个研究点目标入组 40 人开始时间: 2020年3月10日最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
Hours 至 72 Hours(—)
性别
All

入选标准

  • Infants 26 0/7 to 31 6/7 weeks corrected gestational age (gestation at birth plus days since birth)
  • Weight appropriate for gestational age at birth
  • Age < 72 hours
  • Currently on nCPAP with an FiO2 requirement <0.30
  • Approval of treating medical and nursing staff for recruitment to relevant study arm
  • Parent(s) or guardian able and willing to provide informed consent
  • At least one parent or guardian aged 18 years or older at the time of consent
  • Have not yet received a dose of surfactant

排除标准

  • Apgar score less than or equal to 5 at five minutes after birth
  • Both parents of baby under 18 years of age (due to the complexities of obtaining consent).
  • Prior instillation of surfactant
  • Congenital anomaly or syndrome expected to have significant effect on cardio-respiratory function
  • Other diseases interfering with cardiopulmonary functions (hydrops fetalis, toxoplasmosis, rubella, cytomegalovirus, herpes simplex)
  • Known or suspected chromosomal abnormality
  • Concomitant or expected treatment with inhaled nitric oxide
  • Any infant with fragile skin where EIT belt placement or TBS placement may damage the skin.

研究者

发起方
Mater Health

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