跳至主要内容
临床试验/NL-OMON50564
NL-OMON50564已完成不适用

Multicenter study of the performance of Fabian-PRICO for saturation targeting routine use in the NICU - PRICO performance in the NIC

Vyaire Medical0 个研究点目标入组 13 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
入组人数
13

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

年龄范围
0 至 0(—)

入选标准

  • Infants with respiratory insufficiency admitted to the NICU who require
  • respiratory support and supplemental oxygen (FiO2 > 0.21) in one of 4
  • therapeutic categories (HFOV , CMV, Non-Invasive nasal mask, nasal cannula).
  • Informed Consent Form obtained as per EC requirement.

排除标准

  • Not expected to complete 48 hours of the current respiratory support
  • therapeutic category
  • Congenital anomalies
  • Uncontrolled hemodynamics instability
  • Severe airflow obstruction
  • Intracranial hypertension
  • Start of caffeine therapy within 12 hours of entering the study protocol
  • Attending physician does not believe participation of the patient is in their
  • best interest.

研究者

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