NL-OMON30860尚未招募3 期
Assessment of Perinatal Outcome after Sustained Tocolysis in Early Labour (APOSTEL II) - APOSTEL II
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 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
- 年龄范围
- 18 至 99（—）
入选标准
- •Women with a gestational age between 24+0 and 31+6 weeks who are spontaneously in labour, and who have been treated for 48 hours with tocolytics.
排除标准
- •Women with signs of intra-uterine infection, women whose child has signs of fetal distress (abnormal CTG or biophysical profile) or major congenital malformation and women with any contraindication for the use of nifedipine or having a maternal disease (severe hypertension, HELLP syndrome, preeclampsia or other) or other reason for delivery.
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