NL-OMON56856尚未招募不适用
Presepsin to safely reduce antibiotics in preterm infants (PRESAFE trial): a randomized controlled trial with concurrent observational cohort - PRESAFE trial
Amsterdam UMC0 个研究点目标入组 1,266 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 1,266
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
- 0 至 0（—）
入选标准
- •Infants born between 24 and 31+6 weeks gestation are eligible for enrollment.
- •Infants at high- or low-risk of early-onset sepsis will be excluded for
- •randomization and included in the observational part of the study. Infants with
- •moderate risk for EOS are randomized 1:1.
排除标准
- •Infants at low-risk or high-risk for EOS are not eligible for enrollment in the
- •randomization part of the trial.
研究者
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