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临床试验/IRCT2014012716376N1
IRCT2014012716376N1已完成未知

Comparing two methods of cannula nasal with high flow and conventional Fio2 for successful weaning of preterm infants with respiratory distress from Nasal CPAP in Alzahra and Shahidbeheshti hospitals, Isfahan

Vice chancellor for research, Isfahan University of Medical Sciences0 个研究点目标入组 88 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
88

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
28 years 至 37 years(—)
性别
All

入选标准

  • preterm infants with respiratory distress syndrome (RDS) and gestational age (28-37 weeks) who require NCPAP; being stable on NCPAP at Fio2=30% for 6 hours; no clinical sign of RDS such as tachypnea, sever apnea, intercostals retraction and nasal flaring.
  • Exclusion criteria: infants with genetic anomalies; congenital cyanotic heart disease; genetic anomalies in airways or chest; pulmonary hypoplasy; genetic neurologic disease; neuro-mascular disease; inter ventricular hemorrhages (grade 3-4) and hydrocephaly.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research, Isfahan University of Medical Sciences

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Comparing two methods of cannula nasal with high... | 临床试验