IRCT2015103124804N1已完成未知
Adverse kidney effects of standard -daily dosing versus once daily dosing of amikacin among preterm neonates
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 40
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 7 days（—）
- 性别
- All
入选标准
- •Appropriate for gestational age preterm infants with early onset sepsis diagnosis
- •Exclusion criteria:neonates with incomplete treatment ; whom their parents do not accept to be included in this trial ; asphyxia; kidney anomalies in ultrasonography
排除标准
- 未提供
研究者
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