跳至主要内容
临床试验/NL-OMON36929
NL-OMON36929已完成3 期

Does antenatal allopurinol during perinatal asphyxia reduce post-hypoxic-ischemic reperfusion damage in the newborn? A double blind randomised placebo controlled multicenter trial. - ALLO-trial

niversitair Medisch Centrum Utrecht0 个研究点目标入组 220 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
220

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
2 至 99(—)

入选标准

  • Pregnant women with a gestational age of at least 36 weeks, suspicion of fetal distress / intra-uterine asphyxia

排除标准

  • Congenital, chromosomal or syndromal malformations.

研究者

发起方
niversitair Medisch Centrum Utrecht

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