跳至主要内容
临床试验/NL-OMON21183
NL-OMON21183招募中不适用

ong-term follow-up of children exposed in utero to low-dose aspirin for prevention of preterm birth, a 4 year follow-up of the APRIL trial

Amsterdam UMC0 个研究点目标入组 200 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
招募中
发起方
入组人数
200

研究概览

简要总结

n/a

研究设计

研究类型
Observational

入排标准

入选标准

  • All mothers and their child that participated in the APRIL trial. Mortality data of all children up to 4 years will be collected. Surviving children will be assessed at 4 years corrected age (ranging between 45 months and 51 months calculated from the expected date of delivery).

排除标准

  • Women that withdraw their consent after randomization in the original APRIL trial. Women that did not gave consent to be approached for follow-up during the original APRIL trial.

研究者

发起方
Amsterdam UMC

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