ISRCTN88744949已完成不适用
Comparison of effectiveness two Infant Flow modes (Biphasic tr vs NCPAP) in treatment infants = 1250g. A multicentre, randomised controlled trial
Polish Ministry of Science and Higher Education (Poland)0 个研究点目标入组 552 人开始时间: 2010年8月26日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 552
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
- 性别
- All
入选标准
- •1. Study group A (elective):
- •1.1. Preterm newborns (=32 gestational weeks)
- •1.2. Birth weight 500-1250g
- •1.3. Any indications to intubation after birth
- •1.4. Signed informed consent by a parent or legal guardian
- •2. Study group B (weaning):
- •2.1. Preterm newborns (= 32 gestational weeks)
- •2.2. Birth weight 500-1250g
- •2.3. Clinical signs and symptoms of severe RDS
- •2.4. Indications into surfactant administration after delivery
- •2.5. Signed informed consent by a parent or legal guardian
排除标准
- •1. Study group A (elective):
- •1.1. Preterm newborns (>32 gestational weeks)
- •1.2. Birth weight <500 and >1250g
- •1.3. Presence of congenital malformations
- •1.4. APGAR score < 4 (at 5min)
- •1.5. Incidence of air leaks
- •1.6. The lack of written parental consent
- •2. Study group B (weaning):
- •2.1. Preterm newborns (>32 gestational weeks)
- •2.2. Birth weight <500 and >1250g
- •2.3. Presence of congenital malformations
- •2.4. APGAR score < 4 (at 5min)
- •2.5. Incidence of air leaks
- •2.6. The lack of written parental consent
研究者
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