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临床试验/IRCT2013062710279N3
IRCT2013062710279N3已完成3 期

Comparison of prophylactic effect of synbiotic on necrotizing enterocolitis, sepsis and hyperbilirubinemia with placebo on very low birth weight infants

OBEL Pharmacy0 个研究点目标入组 210 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
210

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
1 day 至 1 month(—)
性别
All

入选标准

  • Very low birth weight infants (gestational age: =32 weeks; birth weight: =1500 g) who survived to feed enterally (minimum age: first postnatal day, maximum age: 10 days). Exclusion criteria: Infants who had severe asphyxia (stage III), major congenital anomalies, those who had been fasted for more than 3 weeks, died within the first postnatal 14 days.

排除标准

  • 未提供

研究者

发起方
OBEL Pharmacy

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