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临床试验/NL-OMON29343
NL-OMON29343尚未招募不适用

Immediate Stimulation to Prevent and Inhibit cardioRespiratory Events In preterm infants

one0 个研究点目标入组 16 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
one
入组人数
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Born between 24 weeks 0 days and 29 weeks and 6 days gestation.
  • - First 8 infants: gestational age between 27 weeks and 0 days and 29 weeks and 6 days gestation at start study.
  • - Last 8 infants: gestational age between 24 weeks and 0 days and 26 weeks and 6 days gestation at start study.
  • - Receiving non-invasive respiratory support (NCPAP or NIPPV).
  • - Occurrence of apnea, bradycardia or desaturation of >10 seconds > 1 per hour, but otherwise clinically stable. This can be defined by clinical alarms of the patient monitor and notes of the nurse.
  • - Expected to complete the 48-hour period with non-invasive respiratory support.
  • - Written informed parental consent.

排除标准

  • - Major congenital anomalies that have an adverse effect on breathing or ventilation.
  • - Suspected or proven sepsis
  • - Comfort score >14; comfort is scored by a nurse on 6 items with a 5-point Likert scale. When the sum of these scores is >14 the patient is experiencing discomfort which requires the nurse to look for the cause and, in case it does not improve, provide pain medication.

研究者

发起方
one

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