跳至主要内容
临床试验/ISRCTN25383361
ISRCTN25383361已完成不适用

Antidepressants during pregnancy: risk-benefit study for mother and child

niversity Medical Centre Utrecht (UMCU) (Netherlands)0 个研究点目标入组 400 人开始时间: 2005年12月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
400

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

性别
All

入选标准

  • Women who are pregnant and use one of the modern antidepressants (selective serotonin re-uptake inhibitor [SSRI] and non-SSRI) are included at 16 weeks of pregnancy, group A. Women who stopped taking antidepressants in the first trimester or just before pregnancy are included in group B. Women must be willing and give informed consent and must be able to read in Dutch in order to fill in the questionnaires.

排除标准

  • 1. Co-medication with a similar or higher pregnancy risk factor
  • 2. Alcohol or drug addiction

研究者

发起方
niversity Medical Centre Utrecht (UMCU) (Netherlands)

相似试验