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临床试验/IRCT2015122225650N1
IRCT2015122225650N1已完成未知

The effect of limitation of fluid in treatment of transient tachypnea of newborn

Vice chancellor for research, Babol University of Medical Sciences0 个研究点目标入组 70 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
70

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
no limit 至 no limit(—)
性别
All

入选标准

  • The late preterm (gestational age of 34 – 37 weeks) and term (gestational ageof 37 -42 weeks) and post term (gestational age greater than 42 weeks) neonates with tachypnea (Respiratory Rate greater than 60 per minute) with or without respiratory distress within 6 hours of birth. Exclusion criteria: Pretem neonates (gestational age less than 34 weeks); neonates with history of asphyxia;RDS;air-block syndrom; birth trauma; congenital anomaly and neonates with blood culture positive and also infants who receive surfactants while treatment or develop dehydration complication (weight loss more than one percent daily, reduce urine outflow to lower than (1cc /kg /hour) or increase urine specific gravity more than( 1/017) have excluded from study.

排除标准

  • 未提供

研究者

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

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