跳至主要内容
临床试验/EUCTR2013-005568-24-NL
EUCTR2013-005568-24-NL进行中(未招募)不适用

The reduction of Apneas in Preterm Infants: Low-Flow versus Caffeine - RALFC

Medisch Spectrum Twente0 个研究点开始时间: 2014年5月28日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Preterm infants admitted to the department of neonatology are eligible for the study if they are born between 32 and 36 weeks of gestational age, are considered clinically stable off CPAP and if they experience either 4 or more apneic spells in 3 hours; 4 apneic spells in 12 hours or less or 8 apneic spells in 24 hours or less during the first 10 days after birth.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 290
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • - If other forms of ventilation or continues positive airway pressure is required;
  • - If apneic spells are due to other causes of apnea than Apnea of Prematurity, such as infection, metabolic disturbances, respiratory compromise, cardiovascular disturbances, central nervous system abnormalities, hematologic imbalance, gastrointestinal abnormalities, disturbance in thermoregulation, or side effects of medication;

研究者

相似试验